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

ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT

K Number: K890645 · Decision Mar 8, 1989
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
49
Applicant Total
23
Review Days
28

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Basic Information

Device Name
ESTRADIOL MAIACLONE RADIOIMMUNOASSAY KIT
K Number
K890645
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Serono-Baker Diagnostics, Inc.
Date Received
February 8, 1989
Decision Date
March 8, 1989
Product Code
CHP
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
CHP Radioimmunoassay, Estradiol

Similar 510(k) Clearances

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Other Clearances by Serono-Baker Diagnostics, Inc.

K Number Device Name
K924257 TESTOSTERONE SEROZYME(TM) ENZYME IMMUNOASSAY
K915164 SRI TESTOSTERONE ENZYME IMMUNOASSAY
K914886 SRI(TM) CORTISOL ENZYME IMMUNOASSAY(MAG SOL PHASE)
K915602 SRI DIGOXIN ENZYME IMMUNOASSAY
K912937 SR1 FREE T4 ENZYME IMMUNOASSAY
K914462 SRI PROGESTERONE ENZYME IMMUNOASSAY(MAG SOLD PHAS)
K911912 SR1 T3 UPTAKE ENZYME IMMUNOASSAY(MAG SOLID-PHASE)
K911217 SR1 T4 ENZYME IMMUNOASSAY (MAGNETIC SOLID-PHASE)
K912318 ESTRADIOL SEROZYME ENZYME IMMUNO (MAG SOLID-PHASE)
K911396 SR1 ESTRADIOL ENZYME IMMUNOASSAY
Search all 23 clearances from Serono-Baker Diagnostics, Inc. →