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FDA 510(k)

INTRA V AND SECRET EAR III

K-Number: K930853 · 1993-03-18

ApplicantStarkey Laboratories, Inc.
Decision Date1993-03-18
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INTRA V AND SECRET EAR III 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 1993-03-18 under 510(k) number K930853. 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 INTRA V AND SECRET EAR III?

INTRA V AND SECRET EAR III is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K930853.

When did INTRA V AND SECRET EAR III receive FDA 510(k) clearance?

INTRA V AND SECRET EAR III received FDA 510(k) clearance on 1993-03-18, under 510(k) number K930853.

Who is the listed applicant for INTRA V AND SECRET EAR III?

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 INTRA V AND SECRET EAR III?

The FDA product code for INTRA V AND SECRET EAR III 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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