FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ELECTROPHORESIS REAGENT SET, HDL

K Number: K790791 · Decision Jun 15, 1979
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
7
Applicant Total
32
Review Days
52

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Basic Information

Device Name
ELECTROPHORESIS REAGENT SET, HDL
K Number
K790791
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gelman Sciences, Inc.
Date Received
April 24, 1979
Decision Date
June 15, 1979
Product Code
LBT
Advisory Committee
Clinical Chemistry
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
LBT Electrophoresis, Cholesterol Via Esterase-Oxidase, Hdl

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Other Clearances by Gelman Sciences, Inc.

K Number Device Name
K946190 DRUG DISPENSING SPIKE
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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
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