FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SYRINGE FILTER DEVICES

K Number: K941589 · Decision Sep 6, 1994
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
747
Applicant Total
32
Review Days
159

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Basic Information

Device Name
SYRINGE FILTER DEVICES
K Number
K941589
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gelman Sciences, Inc.
Date Received
March 31, 1994
Decision Date
September 6, 1994
Product Code
FMF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMF Syringe, Piston

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Other Clearances by Gelman Sciences, Inc.

K Number Device Name
K946190 DRUG DISPENSING SPIKE
K943127 PHARMASSURE LARGE VOLUME TRANSFER FILTERS
K941020 DRUG RECONSTITUTION FILTER DEVICE
K942275 VIAL VENT FILTER
K941032 UNKNOWN
K910821 TRANSDUCER PROTECTOR
K892387 MODIFIED GELMAN ARTERIAL FILTER
K884176 CHROMATOGRAPHY KIT
K884178 DRUG CONTROL SET
K884177 DRUG STANDARD SET
Search all 32 clearances from Gelman Sciences, Inc. →