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FDA 510(k)

EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS

K-Number: K960494 · 1996-03-01

ApplicantStarkey Laboratories, Inc.
Decision Date1996-03-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS is the device name listed in this FDA 510(k) record. The listed applicant is Starkey Laboratories, Inc.. It received FDA 510(k) clearance on 1996-03-01 under 510(k) number K960494. 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 EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS?

EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS is a medical device that received FDA 510(k) clearance on 1996-03-01. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K960494.

When did EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS receive FDA 510(k) clearance?

EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS received FDA 510(k) clearance on 1996-03-01, under 510(k) number K960494.

Who is the listed applicant for EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS?

The FDA 510(k) record lists Starkey Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS?

The FDA product code for EUROLINE A312 SERIES OF BEHIND THE EAR AIR CONDUCTION HEARING AIDS is ESD.

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Related Devices (Code: ESD)

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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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