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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Retractor
510(k) Number K874243
Device Name ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000
Applicant
PILLING CO.
420 DELAWARE DR.
FORT WASHINGTON,  PA  19034
Applicant Contact LELAND J WIMER
Correspondent
PILLING CO.
420 DELAWARE DR.
FORT WASHINGTON,  PA  19034
Correspondent Contact LELAND J WIMER
Regulation Number878.4800
Classification Product Code
GAD  
Date Received10/16/1987
Decision Date 11/13/1987
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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