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FDA 510(k)

ENDOSONICS TRAK BACK DEVICE

K-Number: K990271 · 1999-08-30

ApplicantEndosonics Corp.
Decision Date1999-08-30
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENDOSONICS TRAK BACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Endosonics Corp.. It received FDA 510(k) clearance on 1999-08-30 under 510(k) number K990271. 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 ENDOSONICS TRAK BACK DEVICE?

ENDOSONICS TRAK BACK DEVICE is a medical device that received FDA 510(k) clearance on 1999-08-30. The listed applicant is Endosonics Corp.. The 510(k) number is K990271.

When did ENDOSONICS TRAK BACK DEVICE receive FDA 510(k) clearance?

ENDOSONICS TRAK BACK DEVICE received FDA 510(k) clearance on 1999-08-30, under 510(k) number K990271.

Who is the listed applicant for ENDOSONICS TRAK BACK DEVICE?

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

What is the FDA product code for ENDOSONICS TRAK BACK DEVICE?

The FDA product code for ENDOSONICS TRAK BACK DEVICE is DQX.

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Other records listing Endosonics Corp. as applicant

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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