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FDA 510(k)

EUROSTAR SUPER, EUROSTAR VFC

K-Number: K942036 · 1994-06-24

ApplicantStarkey Laboratories, Inc.
Decision Date1994-06-24
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EUROSTAR SUPER, EUROSTAR VFC 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 1994-06-24 under 510(k) number K942036. 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 EUROSTAR SUPER, EUROSTAR VFC?

EUROSTAR SUPER, EUROSTAR VFC is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K942036.

When did EUROSTAR SUPER, EUROSTAR VFC receive FDA 510(k) clearance?

EUROSTAR SUPER, EUROSTAR VFC received FDA 510(k) clearance on 1994-06-24, under 510(k) number K942036.

Who is the listed applicant for EUROSTAR SUPER, EUROSTAR VFC?

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 EUROSTAR SUPER, EUROSTAR VFC?

The FDA product code for EUROSTAR SUPER, EUROSTAR VFC is 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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