Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · CFR · Title 21 — Food and Drugs · Part 878 — General and Plastic Surgery Devices · § 878.4685

§ 878.4685. Extracorporeal shock wave device for treatment of chronic wounds.

258 words·~1 min read·/us/cfr/t21/s§ 878.4685·

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

(a)Identification. An extracorporeal shock wave device for treatment of chronic wounds is a prescription device that focuses acoustic shock waves onto the dermal tissue. The shock waves are generated inside the device and transferred to the body using an acoustic interface.
(b)Classification. Class II (special controls). The special controls for this device are:
(1)Non-clinical performance testing must be conducted to demonstrate that the system produces anticipated and reproducible acoustic pressure shock waves.
(2)The patient-contacting components of the device must be demonstrated to be biocompatible.
(3)Performance data must demonstrate that the reusable components of the device can be reprocessed for subsequent use.
(4)Performance data must be provided to demonstrate the electromagnetic compatibility and electrical safety of the device.
(5)Software verification, validation, and hazard analysis must be performed.
(6)Performance data must support the use life of the system by demonstrating continued system functionality over the labeled use life.
(7)Physician labeling must include:
(i)Information on how the device operates and the typical course of treatment;
(ii)A detailed summary of the device's technical parameters;
(iii)Validated methods and instructions for reprocessing of any reusable components; and
(iv)Instructions for preventing hearing loss by use of hearing protection.
(8)Patient labeling must include:
(i)Relevant contraindications, warnings, precautions, adverse effects, and complications;
(ii)Information on how the device operates and the typical course of treatment;
(iii)The probable risks and benefits associated with the use of the device;
(iv)Post-procedure care instructions; and
(v)Alternative treatments. [83 FR 9699, Mar. 7, 2018]
Connections1 cite this
Cited by 1 section
Citation graph
cites case law
§ 878.4685
Extracorporeal shock wave device for treatment of chronic wounds.
Fed. Reg.×1
Cites 0Cited by 1 across 1 source
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.