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

TERUMO SENSIBEAD THYROXINE EIA KIT

K Number: K841601 · Decision May 22, 1984
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
85
Applicant Total
143
Review Days
34

Basic Information

Device Name
TERUMO SENSIBEAD THYROXINE EIA KIT
K Number
K841601
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1700
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
TERUMO MEDICAL CORP.
Date Received
April 18, 1984
Decision Date
May 22, 1984
Product Code
KLI
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
KLI Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine

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Other Clearances by TERUMO MEDICAL CORP.

K Number Device Name
K111606 PINNACLE PRECISION ACCESS SYSTEM
K111556 GLIDECROSS SUPPORT CATHETER
K110540 TERUMO SUPPORT CATHETER
K102008 GLIDESHEATH
K091329 PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
K082997 TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
K090040 RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
K082847 PINNACLE ROII INTRODUCER SHEATH
K082519 FINECROSS MG CORONARY MICRO-GUIDE CATHETER
K082736 RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
Search all 143 clearances from TERUMO MEDICAL CORP. →