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

VIAL VENT FILTER

K Number: K942275 · Decision Jul 26, 1994
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
32
Review Days
77

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Basic Information

Device Name
VIAL VENT FILTER
K Number
K942275
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gelman Sciences, Inc.
Date Received
May 10, 1994
Decision Date
July 26, 1994
Product Code
FPB
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
FPB Filter, Infusion Line

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Other Clearances by Gelman Sciences, Inc.

K Number Device Name
K946190 DRUG DISPENSING SPIKE
K943127 PHARMASSURE LARGE VOLUME TRANSFER FILTERS
K941589 SYRINGE FILTER DEVICES
K941020 DRUG RECONSTITUTION FILTER DEVICE
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. →