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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Operating-Room, Ac-Powered
510(k) Number K831086
Device Name CEILING MOUNTED SUPPORT
Applicant
Amsco Co.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Amsco Co.
4221 Richmond Rd., NW
Walker,  MI  49534
Regulation Number878.4960
Classification Product Code
FQO  
Date Received04/04/1983
Decision Date 08/12/1983
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
Predetermined Change
Control Plan Authorized		 No
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