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

CHROMATOGRAPHY KIT

K Number: K884176 · Decision Apr 4, 1989
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
4
Applicant Total
32
Review Days
182

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Basic Information

Device Name
CHROMATOGRAPHY KIT
K Number
K884176
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2270
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gelman Sciences, Inc.
Date Received
October 4, 1988
Decision Date
April 4, 1989
Product Code
DPA
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DPA Apparatus, General Use, Thin Layer Chromatography

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DPA), ordered by most recent decision date.

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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
K884178 DRUG CONTROL SET
K884177 DRUG STANDARD SET
Search all 32 clearances from Gelman Sciences, Inc. →