AIROS 6 Sequential Compression Device— 510(k) K193069

Substantially Equivalent

Airos Medical, Inc.

FDA 510(k) clearance K193069 for AIROS 6 Sequential Compression Device, Substantially Equivalent on 2019-12-04. Applicant: Airos Medical, Inc..

Clearance details

Applicant: Airos Medical, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2019-11-04
Decision date: 2019-12-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Audubon, PA, US

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