FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

AUTOSTAT II ANA SCREEN ELISA

K Number: K983655 · Decision Jan 28, 1999
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
111
Applicant Total
31
Review Days
101

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Basic Information

Device Name
AUTOSTAT II ANA SCREEN ELISA
K Number
K983655
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cogent Diagnotics , Ltd.
Date Received
October 19, 1998
Decision Date
January 28, 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 Cogent Diagnotics , Ltd.

K Number Device Name
K003054 AUTOSTAT II ENA-6 PROFILE ELISA
K003057 AUTOSTAT II ENA-4 PROFILE ELISA
K002215 AUTOSTAT II ANTI-MYELOPEROXIDASE (MPO) ELISA
K993557 AUTOSTAT II RHEUMATOID FACTOR IGA ELISA
K994338 AUTOSTAT II RHEUMATOID FACTOR IGM ELISA
K993085 AUTOSTAT II ANTI-CARDIOLIPIN SCREEN ELISA
K993304 AUTOSTAT II RHEUMATOID FACTOR IGG ELISA
K992449 AUTOSTAT II ANTI-CARDIOLIPIN IGM ELISA
K993086 AUTOSTAT II ANTI-GLIADIN IGA ELISA
K993087 AUTOSTAT II ANTI-GLIADIN IGG ELISA
Search all 31 clearances from Cogent Diagnotics , Ltd. →