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FDA 510(k)

STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES

K-Number: K880969 · 1988-04-11

ApplicantStarkey Laboratories, Inc.
Decision Date1988-04-11
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES 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 1988-04-11 under 510(k) number K880969. 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 STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES?

STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES is a medical device that received FDA 510(k) clearance on 1988-04-11. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K880969.

When did STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES receive FDA 510(k) clearance?

STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES received FDA 510(k) clearance on 1988-04-11, under 510(k) number K880969.

Who is the listed applicant for STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES?

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 STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES?

The FDA product code for STAR 22,33,66 SERIES & STARKEY H. AND SM SERIES is ESD.

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Other records listing Starkey Laboratories, Inc. as applicant

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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.

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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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