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FDA 510(k)

VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193

K-Number: K851479 · 1985-06-14

ApplicantVygon Corp.
Decision Date1985-06-14
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193 is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1985-06-14 under 510(k) number K851479. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193?

VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193 is a medical device that received FDA 510(k) clearance on 1985-06-14. The listed applicant is Vygon Corp.. The 510(k) number is K851479.

When did VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193 receive FDA 510(k) clearance?

VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193 received FDA 510(k) clearance on 1985-06-14, under 510(k) number K851479.

Who is the listed applicant for VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193?

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 BALLOON FOR IDENTIFICATION OF EPIDURAL 193?

The FDA product code for VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193 is CAZ.

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Other records listing Vygon Corp. as applicant

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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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