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FDA 510(k)

A.V. FISTULA CANNULATION SETS

K-Number: K830021 · 1983-01-14

ApplicantTravenol Laboratories, S.A.
Decision Date1983-01-14
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

A.V. FISTULA CANNULATION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K830021. 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 A.V. FISTULA CANNULATION SETS?

A.V. FISTULA CANNULATION SETS is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K830021.

When did A.V. FISTULA CANNULATION SETS receive FDA 510(k) clearance?

A.V. FISTULA CANNULATION SETS received FDA 510(k) clearance on 1983-01-14, under 510(k) number K830021.

Who is the listed applicant for A.V. FISTULA CANNULATION SETS?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A.V. FISTULA CANNULATION SETS?

The FDA product code for A.V. FISTULA CANNULATION SETS is KOC.

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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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