FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

AESKULISA MPO, MODEL 30-7303US

K Number: K091860 · Decision Feb 23, 2010
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
73
Applicant Total
8
Review Days
249

Basic Information

Device Name
AESKULISA MPO, MODEL 30-7303US
K Number
K091860
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
AESKU.DIAGNOSTICS
Date Received
June 19, 2009
Decision Date
February 23, 2010
Product Code
MOB
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
MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

Similar 510(k) Clearances

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

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Other Clearances by AESKU.DIAGNOSTICS

K Number Device Name
K132082 AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECK
K091859 AESKU PR3
K081251 MODIFICATION TO AESKULISA DS DNA G
K081104 AESKULISA ANA HEP-2, REF 30-7115US
K052439 AESKULISA GLIA A AND AESKULISA GLIA G
K041628 AESKULISA DS DNA G
K041753 AESKULISA ENA 6 S