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

DRUG STANDARD SET

K Number: K884177 · Decision Feb 17, 1989
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
93
Applicant Total
32
Review Days
136

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Basic Information

Device Name
DRUG STANDARD SET
K Number
K884177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3200
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Gelman Sciences, Inc.
Date Received
October 4, 1988
Decision Date
February 17, 1989
Product Code
DKB
Advisory Committee
Clinical Toxicology
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
DKB Calibrators, Drug Mixture

Similar 510(k) Clearances

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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. →