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

MEDIX BIOTECH LH ENZYME IMMUNOASSAY TEST KIT

K Number: K873668 · Decision Oct 7, 1987
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
39
Review Days
27

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Basic Information

Device Name
MEDIX BIOTECH LH ENZYME IMMUNOASSAY TEST KIT
K Number
K873668
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Medix Biotech, Inc.
Date Received
September 10, 1987
Decision Date
October 7, 1987
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

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Other Clearances by Medix Biotech, Inc.

K Number Device Name
K952873 MEDIX BIOTECH STREP A ANTIGEN DETECTION TEST (MODIFICATION)
K952319 CONTRAST & RAPID HCG URINE/SERUM TST
K932482 MEDIX BIOTECH BESTEST STREP A CAT. NO. BSF1010
K932758 MEDIX BIOTECH BESTEST HCG-URINE TEST KIT
K925436 MEDIX BIOTECH TOTAL T3 ENZYME IMMUNOASSAY TEST KIT
K924259 MEDIX BIOTECH BESTEST(TM) HCG-URINE, CAT# B1H0100
K922047 IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064
K921700 TSH ENZYME IMMUNOASSAY TEST KIT CAT. NO. KIF4093
K920712 MEDIX BIOTECH THROXINE ENZYME IMMUNOASSAY TEST KIT
K920345 PROLACTIN ENZYME IMMUNOASSAY TEST KIT (MODIFIED)
Search all 39 clearances from Medix Biotech, Inc. →