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

GELMAN IG-FIX KIT

K Number: K812253 · Decision Sep 1, 1981
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
53
Applicant Total
32
Review Days
21

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Basic Information

Device Name
GELMAN IG-FIX KIT
K Number
K812253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Gelman Sciences, Inc.
Date Received
August 11, 1981
Decision Date
September 1, 1981
Product Code
CZP
Advisory Committee
Immunology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CZP Iga, Antigen, Antiserum, Control

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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
K942275 VIAL VENT FILTER
K941032 UNKNOWN
K910821 TRANSDUCER PROTECTOR
K892387 MODIFIED GELMAN ARTERIAL FILTER
K884176 CHROMATOGRAPHY KIT
K884178 DRUG CONTROL SET
Search all 32 clearances from Gelman Sciences, Inc. →