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FDA 510(k) Application Details - K010477
Device Classification Name
Syringe, Antistick
More FDA Info for this Device
510(K) Number
K010477
Device Name
Syringe, Antistick
Applicant
AUTO-LOCK
58 OAKDALE AVE.
SAN RAFAEL, CA 94901 US
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Contact
DIETRICH W GRABIS
Other 510(k) Applications for this Contact
Regulation Number
880.5860
More FDA Info for this Regulation Number
Classification Product Code
MEG
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/20/2001
Decision Date
10/09/2001
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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