AIROS 8 Sequential Compression Device
K-Number: K172779 · 2018-06-22
Device Summary
Frequently Asked Questions
What is the AIROS 8 Sequential Compression Device?
AIROS 8 Sequential Compression Device is a medical device that received FDA 510(k) clearance on 2018-06-22. The listed applicant is Airos Medical, Inc.. The 510(k) number is K172779.
When did AIROS 8 Sequential Compression Device receive FDA 510(k) clearance?
AIROS 8 Sequential Compression Device received FDA 510(k) clearance on 2018-06-22, under 510(k) number K172779.
Who is the listed applicant for AIROS 8 Sequential Compression Device?
The FDA 510(k) record lists Airos Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AIROS 8 Sequential Compression Device?
The FDA product code for AIROS 8 Sequential Compression Device is JOW.
Other records listing Airos Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JOW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.