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FDA 510(k)

TRAC-WRIGHT TRAC 10 CATHETER

K-Number: K915238 · 1992-02-19

Decision Date1992-02-19
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRAC-WRIGHT TRAC 10 CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1992-02-19 under 510(k) number K915238. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAC-WRIGHT TRAC 10 CATHETER?

TRAC-WRIGHT TRAC 10 CATHETER is a medical device that received FDA 510(k) clearance on 1992-02-19. The listed applicant is Dow Corning Wright. The 510(k) number is K915238.

When did TRAC-WRIGHT TRAC 10 CATHETER receive FDA 510(k) clearance?

TRAC-WRIGHT TRAC 10 CATHETER received FDA 510(k) clearance on 1992-02-19, under 510(k) number K915238.

Who is the listed applicant for TRAC-WRIGHT TRAC 10 CATHETER?

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

What is the FDA product code for TRAC-WRIGHT TRAC 10 CATHETER?

The FDA product code for TRAC-WRIGHT TRAC 10 CATHETER is MCW.

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 Dow Corning Wright 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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Related Devices (Code: MCW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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