Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PHONAK MICROLINK, PERSONAL FM RECEIVER

K-Number: K964035 · 1996-12-04

ApplicantPhonak, Inc.
Decision Date1996-12-04
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PHONAK MICROLINK, PERSONAL FM RECEIVER is the device name listed in this FDA 510(k) record. The listed applicant is Phonak, Inc.. It received FDA 510(k) clearance on 1996-12-04 under 510(k) number K964035. 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 MICROLINK, PERSONAL FM RECEIVER?

PHONAK MICROLINK, PERSONAL FM RECEIVER is a medical device that received FDA 510(k) clearance on 1996-12-04. The listed applicant is Phonak, Inc.. The 510(k) number is K964035.

When did PHONAK MICROLINK, PERSONAL FM RECEIVER receive FDA 510(k) clearance?

PHONAK MICROLINK, PERSONAL FM RECEIVER received FDA 510(k) clearance on 1996-12-04, under 510(k) number K964035.

Who is the listed applicant for PHONAK MICROLINK, PERSONAL FM RECEIVER?

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 MICROLINK, PERSONAL FM RECEIVER?

The FDA product code for PHONAK MICROLINK, PERSONAL FM RECEIVER 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

View on FDA Database →

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

↑