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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 K924700
Device Name FISK HEADREST
Applicant
RHINO MFG.
11321 TRADE CENTER DRIVE, #260
RANCHO CORDOVA,  CA  95742
Applicant Contact SHANE FISK
Correspondent
RHINO MFG.
11321 TRADE CENTER DRIVE, #260
RANCHO CORDOVA,  CA  95742
Correspondent Contact SHANE FISK
Regulation Number878.4960
Classification Product Code
FQO  
Date Received09/17/1992
Decision Date 01/15/1993
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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