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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Curette, Surgical, General Use
510(k) Number K932493
Device Name SURGICAL CURETTE
Applicant
WHITNEY PRODUCTS, INC.
1822 PICKWICK LN.
GLENVIEW,  IL  60025
Applicant Contact WILLIAM WHITNEY
Correspondent
WHITNEY PRODUCTS, INC.
1822 PICKWICK LN.
GLENVIEW,  IL  60025
Correspondent Contact WILLIAM WHITNEY
Regulation Number878.4800
Classification Product Code
FZS  
Date Received05/24/1993
Decision Date 01/07/1994
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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