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FDA 510(k)

WIDEX MODEL LOGO - L9

K-Number: K945703 · 1994-12-23

Decision Date1994-12-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WIDEX MODEL LOGO - L9 is the device name listed in this FDA 510(k) record. The listed applicant is Widex Hearing Aid Co., Inc.. It received FDA 510(k) clearance on 1994-12-23 under 510(k) number K945703. 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 WIDEX MODEL LOGO - L9?

WIDEX MODEL LOGO - L9 is a medical device that received FDA 510(k) clearance on 1994-12-23. The listed applicant is Widex Hearing Aid Co., Inc.. The 510(k) number is K945703.

When did WIDEX MODEL LOGO - L9 receive FDA 510(k) clearance?

WIDEX MODEL LOGO - L9 received FDA 510(k) clearance on 1994-12-23, under 510(k) number K945703.

Who is the listed applicant for WIDEX MODEL LOGO - L9?

The FDA 510(k) record lists Widex Hearing Aid Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIDEX MODEL LOGO - L9?

The FDA product code for WIDEX MODEL LOGO - L9 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 Widex Hearing Aid Co., 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 52 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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