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FDA 510(k) Application Details - K964597
Device Classification Name
Syringe, Piston
More FDA Info for this Device
510(K) Number
K964597
Device Name
Syringe, Piston
Applicant
BIOSURGICAL CORP.
592 ROSSO COURT
PLEASANTON, CA 94566 US
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Contact
JEFFREY M COHEN
Other 510(k) Applications for this Contact
Regulation Number
880.5860
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Classification Product Code
FMF
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More FDA Info for this Product Code
Date Received
11/18/1996
Decision Date
09/08/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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