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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Kit, Surgical Instrument, Disposable
510(k) Number K761193
Device Name SUTURE REMOVAL KIT
Applicant
SUPERIOR PLASTIC PRODUCTS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SUPERIOR PLASTIC PRODUCTS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4800
Classification Product Code
KDD  
Date Received12/06/1976
Decision Date 01/12/1977
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
Recalls CDRH Recalls
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