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FDA 510(k)

MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20

K-Number: K870067 · 1987-04-28

ApplicantVygon Corp.
Decision Date1987-04-28
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20 is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 1987-04-28 under 510(k) number K870067. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20?

MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20 is a medical device that received FDA 510(k) clearance on 1987-04-28. The listed applicant is Vygon Corp.. The 510(k) number is K870067.

When did MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20 receive FDA 510(k) clearance?

MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20 received FDA 510(k) clearance on 1987-04-28, under 510(k) number K870067.

Who is the listed applicant for MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20?

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 MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20?

The FDA product code for MULTICATH - CODE#S 8.1207.OO/8.1208.00/8.1205.20 is DQY.

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Other records listing Vygon Corp. as applicant

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Related Devices (Code: DQY)

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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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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