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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Biopsy Needle
510(k) Number K844993
Device Name COHEN-WARNER TESTICULAR BIOPSY TRAY 2N2720
Applicant
OMNIS SURGICAL, INC.
1 BAXTER PARKWAY 3-2W
DEERFIELD,  IL  60015
Applicant Contact THOMAS D NICKEL
Correspondent
OMNIS SURGICAL, INC.
1 BAXTER PARKWAY 3-2W
DEERFIELD,  IL  60015
Correspondent Contact THOMAS D NICKEL
Regulation Number876.1075
Classification Product Code
FCG  
Date Received12/26/1984
Decision Date 02/28/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
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