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FDA 510(k)

TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107

K-Number: K003276 · 2000-12-01

ApplicantNuMED, Inc.
Decision Date2000-12-01
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107 is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2000-12-01 under 510(k) number K003276. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107?

TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107 is a medical device that received FDA 510(k) clearance on 2000-12-01. The listed applicant is NuMED, Inc.. The 510(k) number is K003276.

When did TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107 receive FDA 510(k) clearance?

TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107 received FDA 510(k) clearance on 2000-12-01, under 510(k) number K003276.

Who is the listed applicant for TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107?

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

What is the FDA product code for TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107?

The FDA product code for TYSHAK MINI PEDIATRIC PTV CATHETER, MODEL 107 is LIT.

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 NuMED, 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.

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Related Devices (Code: LIT)

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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