CRF CHARCOAL CANISTER REPLACEMENT FILTER— 510(k) K920209

Name: FDA 510(k) clearance K920209
Creator: U.S. Food and Drug Administration
Published: 1992-10-01

Substantially Equivalent

Quinn Healthcare Products

FDA 510(k) clearance K920209 for CRF CHARCOAL CANISTER REPLACEMENT FILTER, Substantially Equivalent on 1992-10-01. Applicant: Quinn Healthcare Products. Device class: 2.

Clearance details

Applicant: Quinn Healthcare Products
Product code: Code FYD
Device class: Class 2
Regulation: 21 CFR 878.5070
Advisory panel: General, Plastic Surgery
Date received: 1992-01-16
Decision date: 1992-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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K920210 — SRH-678 VACCUUM TUBING1992-10-01

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