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FDA 510(k)

VYGON LIFEVAC MID-LINE TRAY

K-Number: K954112 · 1996-05-09

ApplicantVygon Corp.
Decision Date1996-05-09
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VYGON LIFEVAC MID-LINE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1996-05-09 under 510(k) number K954112. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON LIFEVAC MID-LINE TRAY?

VYGON LIFEVAC MID-LINE TRAY is a medical device that received FDA 510(k) clearance on 1996-05-09. The listed applicant is Vygon Corp.. The 510(k) number is K954112.

When did VYGON LIFEVAC MID-LINE TRAY receive FDA 510(k) clearance?

VYGON LIFEVAC MID-LINE TRAY received FDA 510(k) clearance on 1996-05-09, under 510(k) number K954112.

Who is the listed applicant for VYGON LIFEVAC MID-LINE TRAY?

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 LIFEVAC MID-LINE TRAY?

The FDA product code for VYGON LIFEVAC MID-LINE TRAY is FOZ.

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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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