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

AUTOSTAT II ANTI-CARDIOLIPIN IGM ELISA

K Number: K992449 · Decision Nov 24, 1999
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
93
Applicant Total
31
Review Days
125

Basic Information

Device Name
AUTOSTAT II ANTI-CARDIOLIPIN IGM ELISA
K Number
K992449
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
COGENT DIAGNOTICS LTD.
Date Received
July 22, 1999
Decision Date
November 24, 1999
Product Code
MID
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
MID System, Test, Anticardiolipin Immunological

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