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

MEDIX BIOTECH FERRITIN ENZYME IMMUNOASSAY TEST KIT

K Number: K873730 · Decision Nov 4, 1987
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
23
Applicant Total
39
Review Days
50

Basic Information

Device Name
MEDIX BIOTECH FERRITIN ENZYME IMMUNOASSAY TEST KIT
K Number
K873730
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
MEDIX BIOTECH, INC.
Date Received
September 15, 1987
Decision Date
November 4, 1987
Product Code
JMG
Advisory Committee
Immunology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JMG Radioimmunoassay (Two-Site Solid Phase), Ferritin

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K Number Device Name
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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. →