FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TERUMO SENSIBEAD EIA FSH KIT

K Number: K863928 · Decision Dec 4, 1986
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
87
Applicant Total
143
Review Days
57

Basic Information

Device Name
TERUMO SENSIBEAD EIA FSH KIT
K Number
K863928
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
TERUMO MEDICAL CORP.
Date Received
October 8, 1986
Decision Date
December 4, 1986
Product Code
CGJ
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
CGJ Radioimmunoassay, Follicle-Stimulating Hormone

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K Number Device Name
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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. →