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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cap, Surgical
510(k) Number K874066
Device Name SURGICAL CAPS
Applicant
INTERPRO INTL., INC.
2 VIEWPOINT TERRACE
LEBANON,  NJ  08833
Applicant Contact WAYNE R KNUPP
Correspondent
INTERPRO INTL., INC.
2 VIEWPOINT TERRACE
LEBANON,  NJ  08833
Correspondent Contact WAYNE R KNUPP
Regulation Number878.4040
Classification Product Code
FYF  
Date Received10/05/1987
Decision Date 11/04/1987
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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