PHONAK PICONET 232X-AZ HEARING INSTRUMENT
K-Number: K945439 · 1995-08-23
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Device Summary
Frequently Asked Questions
What is the PHONAK PICONET 232X-AZ HEARING INSTRUMENT?
PHONAK PICONET 232X-AZ HEARING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1995-08-23. The listed applicant is Phonak, Inc.. The 510(k) number is K945439.
When did PHONAK PICONET 232X-AZ HEARING INSTRUMENT receive FDA 510(k) clearance?
PHONAK PICONET 232X-AZ HEARING INSTRUMENT received FDA 510(k) clearance on 1995-08-23, under 510(k) number K945439.
Who is the listed applicant for PHONAK PICONET 232X-AZ HEARING INSTRUMENT?
The FDA 510(k) record lists Phonak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHONAK PICONET 232X-AZ HEARING INSTRUMENT?
The FDA product code for PHONAK PICONET 232X-AZ HEARING INSTRUMENT is ESD.
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 Phonak, Inc. 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: ESD)
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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