AIROS 6 Sequential Compression Device
K-Number: K193069 · 2019-12-04
ApplicantAiros Medical, Inc.
Decision Date2019-12-04
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
AIROS 6 Sequential Compression Device is a medical device manufactured by Airos Medical, Inc.. It received FDA 510(k) clearance on 2019-12-04 under approval number K193069. 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 6 Sequential Compression Device?
AIROS 6 Sequential Compression Device is a medical device that received FDA 510(k) clearance on 2019-12-04. It is manufactured by Airos Medical, Inc.. The 510(k) number is K193069.
When was AIROS 6 Sequential Compression Device approved by the FDA?
AIROS 6 Sequential Compression Device received FDA 510(k) clearance on 2019-12-04, under approval number K193069.
What company makes AIROS 6 Sequential Compression Device?
AIROS 6 Sequential Compression Device is manufactured by Airos Medical, Inc..
What is the FDA product code for AIROS 6 Sequential Compression Device?
The FDA product code for AIROS 6 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.