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

MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT

K Number: K854379 · Decision Jan 7, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
13
Review Days
69

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Basic Information

Device Name
MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT
K Number
K854379
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bioclinical Systems, Inc.
Date Received
October 30, 1985
Decision Date
January 7, 1986
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

Similar 510(k) Clearances

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

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Other Clearances by Bioclinical Systems, Inc.

K Number Device Name
K950196 CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIA
K945911 CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARS
K933122 MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGAR
K933121 MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGAR
K873086 ROUND 1
K860334 VISI-CHECK HLH TEST MONOCLONAL
K860333 MICRO-ELISA HLH TEST KIT MONOCLONAL
K855227 MICRO-EIA THEOPHYLLINE TEST KIT MONOCLONAL
K854059 MICRO-ELISA HCG EST KIT VISI-CHECK HCG TEST KIT NO
K850257 BCS GLUCOSE COLORIMETRIC TEST
Search all 13 clearances from Bioclinical Systems, Inc. →