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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Retractor
510(k) Number K853796
Device Name RAYLOR RETRACTORS
Applicant
CEDAR SURGICAL, INC.
11 CHARLES LAKE RD.
NORTH OAKS,  MN  55110
Applicant Contact FRED S HALVERSON
Correspondent
CEDAR SURGICAL, INC.
11 CHARLES LAKE RD.
NORTH OAKS,  MN  55110
Correspondent Contact FRED S HALVERSON
Regulation Number878.4800
Classification Product Code
GAD  
Date Received09/11/1985
Decision Date 10/07/1985
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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