ARTAIRA Arterial Compression Device (AACD01)— 510(k) K240499

Substantially Equivalent

Airos Medical, Inc.

FDA 510(k) clearance K240499 for ARTAIRA Arterial Compression Device (AACD01), Substantially Equivalent on 2024-10-11. Applicant: Airos Medical, Inc..

Clearance details

Applicant: Airos Medical, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2024-02-20
Decision date: 2024-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Audubon, PA, US

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