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FDA 510(k)

TURBO TRACKER

K-Number: K960806 · 1996-05-02

ApplicantTarget Therapeutics
Decision Date1996-05-02
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TURBO TRACKER is the device name listed in this FDA 510(k) record. The listed applicant is Target Therapeutics. It received FDA 510(k) clearance on 1996-05-02 under 510(k) number K960806. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBO TRACKER?

TURBO TRACKER is a medical device that received FDA 510(k) clearance on 1996-05-02. The listed applicant is Target Therapeutics. The 510(k) number is K960806.

When did TURBO TRACKER receive FDA 510(k) clearance?

TURBO TRACKER received FDA 510(k) clearance on 1996-05-02, under 510(k) number K960806.

Who is the listed applicant for TURBO TRACKER?

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 TURBO TRACKER?

The FDA product code for TURBO TRACKER is DQO.

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Related Devices (Code: DQO)

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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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