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FDA 510(k)

ECHOSIGHT STENT SET

K-Number: K914280 · 1992-01-09

Decision Date1992-01-09
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ECHOSIGHT STENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1992-01-09 under 510(k) number K914280. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHOSIGHT STENT SET?

ECHOSIGHT STENT SET is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Cook Urological, Inc.. The 510(k) number is K914280.

When did ECHOSIGHT STENT SET receive FDA 510(k) clearance?

ECHOSIGHT STENT SET received FDA 510(k) clearance on 1992-01-09, under 510(k) number K914280.

Who is the listed applicant for ECHOSIGHT STENT SET?

The FDA 510(k) record lists Cook Urological, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECHOSIGHT STENT SET?

The FDA product code for ECHOSIGHT STENT SET is FAD.

Related Clinical Trials

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.

Other records listing Cook Urological, Inc. 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.

View all 104 devices →

Related Devices (Code: FAD)

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.

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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