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

AESKULISA CARDIOLIPIN AGM

K Number: K040463 · Decision May 12, 2004
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
93
Applicant Total
6
Review Days
79

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Basic Information

Device Name
AESKULISA CARDIOLIPIN AGM
K Number
K040463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Aesku, Inc.
Date Received
February 23, 2004
Decision Date
May 12, 2004
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

Similar 510(k) Clearances

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

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Other Clearances by Aesku, Inc.

K Number Device Name
K062217 AESKULSKA BETA2-GLYCO-A
K051492 AESKULISA ASCA A
K042644 AESKULISA TTG A AND AESKULISA TTG G
K040953 AESKULISA ANA HEP-2
K032469 AESKULISA ANA 8PRO