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FDA 510(k)

VESSEL TIPS, SIZES 13-18

K-Number: K810257 · 1981-03-13

ApplicantQuinton, Inc.
Decision Date1981-03-13
Product CodeFKW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VESSEL TIPS, SIZES 13-18 is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1981-03-13 under 510(k) number K810257. The device is classified under product code FKW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VESSEL TIPS, SIZES 13-18?

VESSEL TIPS, SIZES 13-18 is a medical device that received FDA 510(k) clearance on 1981-03-13. The listed applicant is Quinton, Inc.. The 510(k) number is K810257.

When did VESSEL TIPS, SIZES 13-18 receive FDA 510(k) clearance?

VESSEL TIPS, SIZES 13-18 received FDA 510(k) clearance on 1981-03-13, under 510(k) number K810257.

Who is the listed applicant for VESSEL TIPS, SIZES 13-18?

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

What is the FDA product code for VESSEL TIPS, SIZES 13-18?

The FDA product code for VESSEL TIPS, SIZES 13-18 is FKW.

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Related Devices (Code: FKW)

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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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