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

T3 SEROZYME ENZYMEIMMUNOASSAY KIT, MAG SOLID PHASE

K Number: K880388 · Decision Mar 3, 1988
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
25
Review Days
35

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Basic Information

Device Name
T3 SEROZYME ENZYMEIMMUNOASSAY KIT, MAG SOLID PHASE
K Number
K880388
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Serono Diagnostics, Inc.
Date Received
January 28, 1988
Decision Date
March 3, 1988
Product Code
CDP
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
CDP Radioimmunoassay, Total Triiodothyronine

Similar 510(k) Clearances

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

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Other Clearances by Serono Diagnostics, Inc.

K Number Device Name
K953598 SERIES 9100 PLUS AUTOMATED DIFFERENTIAL HEMATOLOGY ANALYZERS
K942051 SR1 DHEA-S ENZYME IMMUNOASSAY
K883085 T3 UPTAKE SEROZYME ENZYME IMMUNO KT/MAG SOLID PHAS
K882340 LH SEROZYME IMMUNOENZYMETRIC ASSAY KIT,MAG SOL PHA
K874866 T4 SEROZYME ENZYMEIMMUNOASSAY KIT/MAG. SOLID PHASE
K873431 PROGESTERONE MAIA RADIOIMMUNO ASSAY KIT MAG SLD PH
K873186 LH MAIACLONE IMMUNORADIO. ASSAY KIT, MAG SOLID PHA
K873400 PROLACTIN MAIACLONE IMMUNORADIO. KIT, MAG SOL PHA
K872862 PRL SEROZYME IMMUNOENZ. ASSAY KIT, MAG. SOLID PHAS
K873033 HCG SEROZYME IMMUNOENZYM ASSAY KIT/MAG SOLID PHASE
Search all 25 clearances from Serono Diagnostics, Inc. →