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

DAC-CEL T3

K Number: K791232 · Decision Sep 4, 1979
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
17
Review Days
64

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Basic Information

Device Name
DAC-CEL T3
K Number
K791232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Burroughs Wellcome Co.
Date Received
July 2, 1979
Decision Date
September 4, 1979
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

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Other Clearances by Burroughs Wellcome Co.

K Number Device Name
K820069 WELLCOGEN GROUP B
K813508 SAC-CEL
K810215 DAC-CEL HCG
K810214 DAC-CEL DIAGNATAL
K810213 DAC-CEL TSH
K810212 DAC-CEL T3 UPTAKE
K791231 DAC-CEL T4
K781607 STREP-TEX
K780873 THYMUNE-M
K780874 THYMUNE-T
Search all 17 clearances from Burroughs Wellcome Co. →