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FDA 510(k)

PHONAK SONA P2

K-Number: K961653 · 1996-05-29

ApplicantPhonak, Inc.
Decision Date1996-05-29
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHONAK SONA P2 is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1996-05-29 under 510(k) number K961653. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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