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

VARELISA RECOMBI ANA PROFILE

K Number: K993109 · Decision Nov 12, 1999
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
111
Applicant Total
18
Review Days
56

Basic Information

Device Name
VARELISA RECOMBI ANA PROFILE
K Number
K993109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHARMACIA & UPJOHN CO.
Date Received
September 17, 1999
Decision Date
November 12, 1999
Product Code
LJM
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
LJM Antinuclear Antibody (Enzyme-Labeled), Antigen, Controls

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Other Clearances by PHARMACIA & UPJOHN CO.

K Number Device Name
K003414 VARELISA TG (THYROGLOBULIN) ANTIBODIES,
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
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. →