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

MICROZYME UNCONJUGATED ESTRIOL ENZYME IMMUNO KIT

K Number: K903359 · Decision Aug 22, 1990
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
41
Applicant Total
37
Review Days
28

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Basic Information

Device Name
MICROZYME UNCONJUGATED ESTRIOL ENZYME IMMUNO KIT
K Number
K903359
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1265
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Immunotech Corp.
Date Received
July 25, 1990
Decision Date
August 22, 1990
Product Code
CGI
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
CGI Radioimmunoassay, Estriol

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Other Clearances by Immunotech Corp.

K Number Device Name
K954188 OPTICLONE IGG1 FITC/IGG2A PE ISOTYPIC CONTROL
K952789 OPTICLONE CD4FITC/CD8 PE MONOCLONAL ANTIBODIES
K950626 OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES
K931228 PROGESTERONE RADIOIMMUNOASSAY KIT
K911634 MICROZYME(TM) FREE T4 ENZYME IMMUNOASSAY TEST
K911153 MICROZYME PHENCYCLIDINE ENZYME IMMUNOASSAY TEST KT
K910411 MICROZYME TSH ENZYME IMMUNOASSAY KIT
K905777 MICROZYME THYROID UPTAKE ENZYME IMMUNOASSAY KIT
K903993 MICROZYME(TM) METHAMPHET/AMPHET ENZYME IMMUNO KIT
K904820 MICROZYME T3 ENZYME IMMUNOASSAY KIT
Search all 37 clearances from Immunotech Corp. →