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

AUTOSTAT II ANTI-GLIADIN IGG ELISA

K Number: K993087 · Decision Nov 12, 1999
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
41
Applicant Total
31
Review Days
58

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
AUTOSTAT II ANTI-GLIADIN IGG ELISA
K Number
K993087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5750
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cogent Diagnotics , Ltd.
Date Received
September 15, 1999
Decision Date
November 12, 1999
Product Code
MST
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
MST Antibodies, Gliadin

Similar 510(k) Clearances

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

View all

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
K992440 AUTOSTAT II ANTI-CARDIOLIPIN IGG ELISA
Search all 31 clearances from Cogent Diagnotics , Ltd. →