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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Cast Removal, Ac-Powered
510(k) Number K873721
Device Name PLASTER VACUUM, 115V MODEL NO. 4183-160
Applicant
Martin Medical
36270 W. 103rd St.
P.O. Box 590
Desoto,  KS  66018
Applicant Contact RANDY KILBURN
Correspondent
Martin Medical
36270 W. 103rd St.
P.O. Box 590
Desoto,  KS  66018
Correspondent Contact RANDY KILBURN
Regulation Number888.5960
Classification Product Code
LGH  
Date Received09/15/1987
Decision Date 12/07/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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