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FDA 510(k) Application Details - K121587
Device Classification Name
Percussor, Powered-Electric
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510(K) Number
K121587
Device Name
Percussor, Powered-Electric
Applicant
CHEEN HOUNG ENT. CO. LTD.
24301 WOODSAGE DRIVE
BONITA SPRINGS, FL 34134 US
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Contact
PAUL DRYDEN
Other 510(k) Applications for this Contact
Regulation Number
868.5665
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Classification Product Code
BYI
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More FDA Info for this Product Code
Date Received
05/31/2012
Decision Date
11/22/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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