PROVOX(TM) VOICE PROSTHESIS
K-Number: K940638 · 1994-06-22
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Device Summary
Frequently Asked Questions
What is the PROVOX(TM) VOICE PROSTHESIS?
PROVOX(TM) VOICE PROSTHESIS is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Atos Medical AB. The 510(k) number is K940638.
When did PROVOX(TM) VOICE PROSTHESIS receive FDA 510(k) clearance?
PROVOX(TM) VOICE PROSTHESIS received FDA 510(k) clearance on 1994-06-22, under 510(k) number K940638.
Who is the listed applicant for PROVOX(TM) VOICE PROSTHESIS?
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(TM) VOICE PROSTHESIS?
The FDA product code for PROVOX(TM) VOICE PROSTHESIS 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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