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

MODIFIED PROLACTIN ENZYME IMMUNOASSAY TEST KIT

K Number: K896641 · Decision Dec 27, 1989
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
79
Applicant Total
39
Review Days
33

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Basic Information

Device Name
MODIFIED PROLACTIN ENZYME IMMUNOASSAY TEST KIT
K Number
K896641
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Medix Biotech, Inc.
Date Received
November 24, 1989
Decision Date
December 27, 1989
Product Code
CFT
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
CFT Radioimmunoassay, Prolactin (Lactogen)

Similar 510(k) Clearances

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

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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. →