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FDA 510(k) Application Details - K962017
Device Classification Name
Injector, Jet, Mechanical-Powered
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510(K) Number
K962017
Device Name
Injector, Jet, Mechanical-Powered
Applicant
AMERICAN JET INJECTOR CORP.
880 ORCHARD LN.
LANSDALE, PA 19446-4520 US
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Contact
ROBERT W HARRINGTON
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Regulation Number
872.4475
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Classification Product Code
EGM
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More FDA Info for this Product Code
Date Received
05/23/1996
Decision Date
07/26/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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