AESKULISA ANA 8PRO— 510(k) K032469

Substantially Equivalent

Aesku, Inc.

FDA 510(k) clearance K032469 for AESKULISA ANA 8PRO, Substantially Equivalent on 2003-12-16. Applicant: Aesku, Inc..

Clearance details

Applicant: Aesku, Inc.
Product code: Code LLL
Advisory panel: Immunology
Date received: 2003-08-11
Decision date: 2003-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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