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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Transfer, Patient, Manual
510(k) Number K792318
Device Name SKIL-CARE TURN AND HOLD PAD
Applicant
Skil-Care Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Skil-Care Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number880.6785
Classification Product Code
FMR  
Date Received11/19/1979
Decision Date 12/20/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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