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

VARELISA TG (THYROGLOBULIN) ANTIBODIES,

K Number: K003414 · Decision Nov 27, 2000
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
91
Applicant Total
18
Review Days
25

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Basic Information

Device Name
VARELISA TG (THYROGLOBULIN) ANTIBODIES,
K Number
K003414
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5870
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pharmacia & Upjohn Co.
Date Received
November 2, 2000
Decision Date
November 27, 2000
Product Code
JZO
Advisory Committee
Immunology
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
JZO System, Test, Thyroid Autoantibody

Similar 510(k) Clearances

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

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Other Clearances by Pharmacia & Upjohn Co.

K Number Device Name
K002556 CEEON EASYSERT INTRAOCULAR LENS INJECTOR, MODEL IMP-1
K000312 VARELISA SM ANTIBODIES
K000132 ALLERGEN IMMUNOCAP, MODELS C74, E89, EX2, EX70, EX71, EX73, FX8, FX9, FX10, FX16, FX73, I72, I75, I76, K71, K73, K81, K8
K993585 VARELISA TPO ANTIBODIES, MODEL 12348/12396
K993388 ALLERGEN IMMUNDOCAP MODELC5, C6, C73, E201, E213, F50, F51,F54, F55, F56, F57, F58, F59, F60, F61, F205, F213, F218, F
K993589 VARELISA RNP ANTIBODIES
K993109 VARELISA RECOMBI ANA PROFILE
K993108 VARELISA RECOMBI ANA SCREEN EIA, MODELS 128 48/ 128 96
K991945 PHARMACIA CAP SYSTEM IGE FEIA, MODEL 10-9395-01
K991048 ALLERGEN IMMUNOCAP, MODELS E7, F93, F94, F95, F203, F204, F208, F209, F210, F214, F216, F235, F237, F242, F255, F259, F2
Search all 18 clearances from Pharmacia & Upjohn Co. →