PHONAK SONA P2
K-Number: K961653 · 1996-05-29
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Device Summary
Frequently Asked Questions
What is the PHONAK SONA P2?
PHONAK SONA P2 is a medical device that received FDA 510(k) clearance on 1996-05-29. The listed applicant is Phonak, Inc.. The 510(k) number is K961653.
When did PHONAK SONA P2 receive FDA 510(k) clearance?
PHONAK SONA P2 received FDA 510(k) clearance on 1996-05-29, under 510(k) number K961653.
Who is the listed applicant for PHONAK SONA P2?
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 SONA P2?
The FDA product code for PHONAK SONA P2 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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