BODY BOOT— 510(k) K940723

Substantially Equivalent

Mark-Clark

FDA 510(k) clearance K940723 for BODY BOOT, Substantially Equivalent on 1994-09-06. Applicant: Mark-Clark. Device class: 1.

Clearance details

Applicant: Mark-Clark
Product code: Code LYU
Device class: Class 1
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1994-02-18
Decision date: 1994-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Topka, KS, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.