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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Radiographic, Tilting
510(k) Number K914417
Device Name MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE
Applicant
Med-Vac, Inc.
P.O. Box 9451
1317 Claytonia Ter.
St. Louis,  MO  63117
Applicant Contact ELLEN M HAVEY
Correspondent
Med-Vac, Inc.
P.O. Box 9451
1317 Claytonia Ter.
St. Louis,  MO  63117
Correspondent Contact ELLEN M HAVEY
Regulation Number892.1980
Classification Product Code
IXR  
Date Received10/03/1991
Decision Date 02/27/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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