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

VISI-CHECK HLH TEST MONOCLONAL

K Number: K860334 · Decision Apr 21, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
13
Review Days
82

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Basic Information

Device Name
VISI-CHECK HLH TEST MONOCLONAL
K Number
K860334
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bioclinical Systems, Inc.
Date Received
January 29, 1986
Decision Date
April 21, 1986
Product Code
CEP
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
CEP Radioimmunoassay, Luteinizing Hormone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CEP), 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
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
K854379 MICRO-ELISA TSH TEST KIT-VISI-CHECK TSH TEST KIT
K850257 BCS GLUCOSE COLORIMETRIC TEST
Search all 13 clearances from Bioclinical Systems, Inc. →