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

VARELISA SM ANTIBODIES

K Number: K000312 · Decision Mar 17, 2000
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
27
Applicant Total
18
Review Days
45

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Basic Information

Device Name
VARELISA SM ANTIBODIES
K Number
K000312
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
February 1, 2000
Decision Date
March 17, 2000
Product Code
LKP
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
LKP Anti-Sm Antibody, Antigen And Control

Similar 510(k) Clearances

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

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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
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. →