AIROS 8P Sequential Compression Device
K-Number: K223193 · 2022-12-09
ApplicantAiros Medical, Inc.
Decision Date2022-12-09
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
AIROS 8P Sequential Compression Device is a medical device manufactured by Airos Medical, Inc.. It received FDA 510(k) clearance on 2022-12-09 under approval number K223193. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AIROS 8P Sequential Compression Device?
AIROS 8P Sequential Compression Device is a medical device that received FDA 510(k) clearance on 2022-12-09. It is manufactured by Airos Medical, Inc.. The 510(k) number is K223193.
When was AIROS 8P Sequential Compression Device approved by the FDA?
AIROS 8P Sequential Compression Device received FDA 510(k) clearance on 2022-12-09, under approval number K223193.
What company makes AIROS 8P Sequential Compression Device?
AIROS 8P Sequential Compression Device is manufactured by Airos Medical, Inc..
What is the FDA product code for AIROS 8P Sequential Compression Device?
The FDA product code for AIROS 8P Sequential Compression Device is JOW.
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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.