FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

CHEMELIA ENZYME IMMUNOASSAY FOR (TSH)

K Number: K873625 · Decision Oct 20, 1987
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
20
Review Days
42

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Basic Information

Device Name
CHEMELIA ENZYME IMMUNOASSAY FOR (TSH)
K Number
K873625
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7360
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Boots-Celltech Diagnostics, Inc.
Date Received
September 8, 1987
Decision Date
October 20, 1987
Product Code
JLM
Advisory Committee
Hematology
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
JLM Isoenzymes, Electrophoretic, Glucose-6-Phosphate Dehydrogenase

Other Clearances by Boots-Celltech Diagnostics, Inc.

K Number Device Name
K871877 IDEIA HERPES SIMPLEX VIRUS TEST
K880799 MODIFIED IDEIA CHLAMYDIA TEST
K880758 SUCROSEP SPECIFIC IMMUNORADIOMETRIC ASSAY
K874875 CHEMELIA FREE THYROXINE(FT4)/ENZYME IMMUNO. (EIA)
K872958 IMAGEN INFLUENZA VIRUS A AND B TESTMI
K872843 OVEIA (TM) DUAL ANALYTE
K872056 MODIFIED (DIRECTIONS FOR USE) FOR IDEIA(TM) TEST
K870602 IMAGEN HERPES SIMPLEX VIRUS (HSV) TYPING TEST
K864998 IDEIA(TM) CHLAMYDIA SPECIMEN COLLECTION KIT
K864539 MODIFIED IMAGEN(TM) CHLAMYDIA TEST
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