FDA 510(k)

ARTERIOVENOUS SETS

K-Number: K790381 · 1979-04-20

ApplicantExtracorporeal Medical Specialities, Inc.

Decision Date1979-04-20

Product CodeKOC

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ARTERIOVENOUS SETS is the device name listed in this FDA 510(k) record. The listed applicant is Extracorporeal Medical Specialities, Inc.. It received FDA 510(k) clearance on 1979-04-20 under 510(k) number K790381. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIOVENOUS SETS?

ARTERIOVENOUS SETS is a medical device that received FDA 510(k) clearance on 1979-04-20. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K790381.

When did ARTERIOVENOUS SETS receive FDA 510(k) clearance?

ARTERIOVENOUS SETS received FDA 510(k) clearance on 1979-04-20, under 510(k) number K790381.

Who is the listed applicant for ARTERIOVENOUS SETS?

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

What is the FDA product code for ARTERIOVENOUS SETS?

The FDA product code for ARTERIOVENOUS SETS is KOC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.