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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name light, surgical, floor standing
510(k) Number K882333
Device Name FLOOR LIGHT
Applicant
COMMERCIAL PRODUCTS & ENGINEERING CO.
5001 KENDRICK, S.E.
GRAND RAPIDS,  MI  49512
Applicant Contact JOHN LOMONACO
Correspondent
COMMERCIAL PRODUCTS & ENGINEERING CO.
5001 KENDRICK, S.E.
GRAND RAPIDS,  MI  49512
Correspondent Contact JOHN LOMONACO
Regulation Number878.4580
Classification Product Code
FSS  
Date Received06/06/1988
Decision Date 06/23/1988
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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