PROVOX FREEHANDS HME, MODEL 7710
K-Number: K022125 · 2002-07-30
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Device Summary
Frequently Asked Questions
What is the PROVOX FREEHANDS HME, MODEL 7710?
PROVOX FREEHANDS HME, MODEL 7710 is a medical device that received FDA 510(k) clearance on 2002-07-30. The listed applicant is Atos Medical AB. The 510(k) number is K022125.
When did PROVOX FREEHANDS HME, MODEL 7710 receive FDA 510(k) clearance?
PROVOX FREEHANDS HME, MODEL 7710 received FDA 510(k) clearance on 2002-07-30, under 510(k) number K022125.
Who is the listed applicant for PROVOX FREEHANDS HME, MODEL 7710?
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 FREEHANDS HME, MODEL 7710?
The FDA product code for PROVOX FREEHANDS HME, MODEL 7710 is EWL.
Related Clinical Trials
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.
Other records listing Atos Medical AB 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: EWL)
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.
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