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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 K923176
Device Name SURGICAL INSTRUMENT KIT, DISPOSABLE
Applicant
ULTI-MED INTL., INC.
1688 GLEN ELLYN RD.
GLENDALE HEIGHTS,  IL  60139
Applicant Contact DAVID INSCO
Correspondent
ULTI-MED INTL., INC.
1688 GLEN ELLYN RD.
GLENDALE HEIGHTS,  IL  60139
Correspondent Contact DAVID INSCO
Regulation Number878.4800
Classification Product Code
KDD  
Date Received06/12/1992
Decision Date 06/17/1993
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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