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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Single Patient Use, Portable, Nonpowered
510(k) Number K822902
Device Name MINI-VAC DRAIN SYSTEM
Applicant
ANGUS MEDICAL CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
ANGUS MEDICAL CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.4680
Classification Product Code
GCY  
Date Received09/29/1982
Decision Date 12/28/1982
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
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