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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K904934
Device Name AUTOMASTER
Applicant
Team Mfg., Inc.
P.O. Box 15427
Augusta,  GA  30919
Applicant Contact RANDOLPH HAROD
Correspondent
Team Mfg., Inc.
P.O. Box 15427
Augusta,  GA  30919
Correspondent Contact RANDOLPH HAROD
Classification Product Code
IPQ
Date Received11/01/1990
Decision Date 05/21/1991
Decision Substantially Equivalent (SESE)
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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