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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Percussor, Powered-Electric
510(k) Number K880597
Device Name THUMPER MODEL P-1000
Applicant
Micro Tek Engineering
8724 Normandy Ln.
Centerville,  OH  45458
Applicant Contact DAVID STARKEY
Correspondent
Micro Tek Engineering
8724 Normandy Ln.
Centerville,  OH  45458
Correspondent Contact DAVID STARKEY
Regulation Number868.5665
Classification Product Code
BYI  
Date Received02/11/1988
Decision Date 03/29/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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