DYNA 231X
K-Number: K950758 · 1995-03-21
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Device Summary
Frequently Asked Questions
What is the DYNA 231X?
DYNA 231X is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Phonak, Inc.. The 510(k) number is K950758.
When did DYNA 231X receive FDA 510(k) clearance?
DYNA 231X received FDA 510(k) clearance on 1995-03-21, under 510(k) number K950758.
Who is the listed applicant for DYNA 231X?
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 DYNA 231X?
The FDA product code for DYNA 231X is ESD.
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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