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FDA 510(k)

SEEKER LITE - 10

K-Number: K922912 · 1992-11-17

ApplicantTarget Therapeutics
Decision Date1992-11-17
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SEEKER LITE - 10 is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1992-11-17 under 510(k) number K922912. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEEKER LITE - 10?

SEEKER LITE - 10 is a medical device that received FDA 510(k) clearance on 1992-11-17. The listed applicant is Target Therapeutics. The 510(k) number is K922912.

When did SEEKER LITE - 10 receive FDA 510(k) clearance?

SEEKER LITE - 10 received FDA 510(k) clearance on 1992-11-17, under 510(k) number K922912.

Who is the listed applicant for SEEKER LITE - 10?

The FDA 510(k) record lists Target Therapeutics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEEKER LITE - 10?

The FDA product code for SEEKER LITE - 10 is DQX.

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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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