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FDA 510(k)

VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW

K-Number: K851480 · 1985-05-07

ApplicantVygon Corp.
Decision Date1985-05-07
Product CodeLAE
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1985-05-07 under 510(k) number K851480. The device is classified under product code LAE. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW?

VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW is a medical device that received FDA 510(k) clearance on 1985-05-07. The listed applicant is Vygon Corp.. The 510(k) number is K851480.

When did VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW receive FDA 510(k) clearance?

VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW received FDA 510(k) clearance on 1985-05-07, under 510(k) number K851480.

Who is the listed applicant for VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW?

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 GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW?

The FDA product code for VYGON GUEDEL AIRWAY 511 VYGON BERMANN/OROPHAR AIRW is LAE.

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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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