FDA 510(k)

VYGON 2 FR EPICUTANEO PUR-CATHETER

K-Number: K993052 · 2000-08-03

Decision Date2000-08-03

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VYGON 2 FR EPICUTANEO PUR-CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 2000-08-03 under 510(k) number K993052. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON 2 FR EPICUTANEO PUR-CATHETER?

VYGON 2 FR EPICUTANEO PUR-CATHETER is a medical device that received FDA 510(k) clearance on 2000-08-03. The listed applicant is Vygon Corp.. The 510(k) number is K993052.

When did VYGON 2 FR EPICUTANEO PUR-CATHETER receive FDA 510(k) clearance?

VYGON 2 FR EPICUTANEO PUR-CATHETER received FDA 510(k) clearance on 2000-08-03, under 510(k) number K993052.

Who is the listed applicant for VYGON 2 FR EPICUTANEO PUR-CATHETER?

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

What is the FDA product code for VYGON 2 FR EPICUTANEO PUR-CATHETER?

The FDA product code for VYGON 2 FR EPICUTANEO PUR-CATHETER is LJS.

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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.