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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Applier, Staple, Surgical,
510(k) Number K915670
Device Name MICROAIRE MODEL 2600
Applicant
Microaire
24971 Ave. Stanford W.
Valencia,  CA  91355
Applicant Contact MOE KHOSRAVI
Correspondent
Microaire
24971 Ave. Stanford W.
Valencia,  CA  91355
Correspondent Contact MOE KHOSRAVI
Regulation Number878.4800
Classification Product Code
GEF  
Date Received12/19/1991
Decision Date 03/18/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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