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

IN VITRO T-3 UPTAKE TEST

K Number: K770480 · Decision Apr 6, 1977
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
92
Applicant Total
27
Review Days
26

Basic Information

Device Name
IN VITRO T-3 UPTAKE TEST
K Number
K770480
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1715
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
CLINICAL ASSAYS, INC.
Date Received
March 11, 1977
Decision Date
April 6, 1977
Product Code
KHQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
KHQ Radioassay, Triiodothyronine Uptake

Similar 510(k) Clearances

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

View all

Other Clearances by CLINICAL ASSAYS, INC.

K Number Device Name
K832712 FOLATE RADIOASSAY KIT CA-1562-125
K832710 VITAMIN B12 RADIOASSAY KIT CA-1534
K832711 VITAMIN B12 FOLATE CA-1515-125
K823476 GAMMADAB LH RADIO-KIT #CA-1508
K823313 IN VITRO GAMMACOAT B-HCG RADIO. TEST
K821611 GAMMADAB [125] FSH RADIOIMMUNAY KIT
K821092 GAMMADAB[125]EGE RADIOIMMUNOASSAY IT
K812227 GAMMACOAT (125) INSULIN RADIOIMMUNOASSAY
K810722 GASTRIN RADIOIMMUNOASSAY TEST
K810967 IN-VITRO TBG RADIOIMMUNOASSAY TEST
Search all 27 clearances from CLINICAL ASSAYS, INC. →