FDA 510(k)

PROVOX MICRON HME

K-Number: K072582 · 2008-05-30

Decision Date2008-05-30

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

PROVOX MICRON HME is the device name listed in this FDA 510(k) record. The listed applicant is Atos Medical AB. It received FDA 510(k) clearance on 2008-05-30 under 510(k) number K072582. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROVOX MICRON HME?

PROVOX MICRON HME is a medical device that received FDA 510(k) clearance on 2008-05-30. The listed applicant is Atos Medical AB. The 510(k) number is K072582.

When did PROVOX MICRON HME receive FDA 510(k) clearance?

PROVOX MICRON HME received FDA 510(k) clearance on 2008-05-30, under 510(k) number K072582.

Who is the listed applicant for PROVOX MICRON HME?

The FDA 510(k) record lists Atos Medical AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROVOX MICRON HME?

The FDA product code for PROVOX MICRON HME is JOH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.