KELLY-WICK TANNELER— 510(k) K830471

Name: FDA 510(k) clearance K830471
Creator: U.S. Food and Drug Administration
Published: 1983-03-24

Substantially Equivalent

Intl. Medical Prosthetics Research

FDA 510(k) clearance K830471 for KELLY-WICK TANNELER, Substantially Equivalent on 1983-03-24. Applicant: Intl. Medical Prosthetics Research. Device class: 1.

Clearance details

Applicant: Intl. Medical Prosthetics Research
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1983-02-15
Decision date: 1983-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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