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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Exhaust, Surgical
510(k) Number K920209
Device Name CRF CHARCOAL CANISTER REPLACEMENT FILTER
Applicant
Quinn Healthcare Products
1120 G. St. NW
Washington,  DC  20005
Applicant Contact SAMIA N RODRIGUEZ
Correspondent
Quinn Healthcare Products
1120 G. St. NW
Washington,  DC  20005
Correspondent Contact SAMIA N RODRIGUEZ
Regulation Number878.5070
Classification Product Code
FYD  
Date Received01/16/1992
Decision Date 10/01/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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