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FDA 510(k)

VYGON STOPCOCKS & RAMPS(MANIFOLDS)

K-Number: K813141 · 1981-11-27

ApplicantExco, Inc.
Decision Date1981-11-27
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VYGON STOPCOCKS & RAMPS(MANIFOLDS) is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1981-11-27 under 510(k) number K813141. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VYGON STOPCOCKS & RAMPS(MANIFOLDS)?

VYGON STOPCOCKS & RAMPS(MANIFOLDS) is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is Exco, Inc.. The 510(k) number is K813141.

When did VYGON STOPCOCKS & RAMPS(MANIFOLDS) receive FDA 510(k) clearance?

VYGON STOPCOCKS & RAMPS(MANIFOLDS) received FDA 510(k) clearance on 1981-11-27, under 510(k) number K813141.

Who is the listed applicant for VYGON STOPCOCKS & RAMPS(MANIFOLDS)?

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

What is the FDA product code for VYGON STOPCOCKS & RAMPS(MANIFOLDS)?

The FDA product code for VYGON STOPCOCKS & RAMPS(MANIFOLDS) is DTL.

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Related Devices (Code: DTL)

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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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