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

TRIA-PEG RIA DIAG. KIT

K Number: K780292 · Decision Mar 2, 1978
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
143
Applicant Total
22
Review Days
9

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Basic Information

Device Name
TRIA-PEG RIA DIAG. KIT
K Number
K780292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1710
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Nuclear Diagnostics, Inc.
Date Received
February 21, 1978
Decision Date
March 2, 1978
Product Code
CDP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
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

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K862312 ENZLIPASE, ENZYMATIC LIPASE KIT
K860472 NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESS
K861735 TIPSEP-TBG ASSAY
K852291 TIPSEP DIGOXIN RIA
K833713 SERUM THYROTROPIN ASSAY KIT, TIPSEP-
K823860 NUCLIPASE (I125) PANCREATIC LIPASE
K811558 TSH-P.E.G.
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