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FDA 510(k)

BOSCH EUROSTAR

K-Number: K933988 · 1993-10-07

ApplicantStarkey Laboratories, Inc.
Decision Date1993-10-07
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BOSCH EUROSTAR 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 1993-10-07 under 510(k) number K933988. 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 BOSCH EUROSTAR?

BOSCH EUROSTAR is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K933988.

When did BOSCH EUROSTAR receive FDA 510(k) clearance?

BOSCH EUROSTAR received FDA 510(k) clearance on 1993-10-07, under 510(k) number K933988.

Who is the listed applicant for BOSCH EUROSTAR?

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 BOSCH EUROSTAR?

The FDA product code for BOSCH EUROSTAR is ESD.

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Other records listing Starkey Laboratories, Inc. as applicant

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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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