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FDA 510(k)

POST AURICULAR HEARING AID MODEL PICO SC-H

K-Number: K910028 · 1991-03-08

ApplicantPhonak, Inc.
Decision Date1991-03-08
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

POST AURICULAR HEARING AID MODEL PICO SC-H is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1991-03-08 under 510(k) number K910028. 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 POST AURICULAR HEARING AID MODEL PICO SC-H?

POST AURICULAR HEARING AID MODEL PICO SC-H is a medical device that received FDA 510(k) clearance on 1991-03-08. The listed applicant is Phonak, Inc.. The 510(k) number is K910028.

When did POST AURICULAR HEARING AID MODEL PICO SC-H receive FDA 510(k) clearance?

POST AURICULAR HEARING AID MODEL PICO SC-H received FDA 510(k) clearance on 1991-03-08, under 510(k) number K910028.

Who is the listed applicant for POST AURICULAR HEARING AID MODEL PICO SC-H?

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 POST AURICULAR HEARING AID MODEL PICO SC-H?

The FDA product code for POST AURICULAR HEARING AID MODEL PICO SC-H 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.

View all 37 devices →

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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