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FDA 510(k)

CATHETER VALVES KV 100 & KV 100EH

K-Number: K861699 · 1986-11-19

Decision Date1986-11-19
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER VALVES KV 100 & KV 100EH is the device name listed in this FDA 510(k) record. The listed applicant is Max Staubli , Ltd.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K861699. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER VALVES KV 100 & KV 100EH?

CATHETER VALVES KV 100 & KV 100EH is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Max Staubli , Ltd.. The 510(k) number is K861699.

When did CATHETER VALVES KV 100 & KV 100EH receive FDA 510(k) clearance?

CATHETER VALVES KV 100 & KV 100EH received FDA 510(k) clearance on 1986-11-19, under 510(k) number K861699.

Who is the listed applicant for CATHETER VALVES KV 100 & KV 100EH?

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

What is the FDA product code for CATHETER VALVES KV 100 & KV 100EH?

The FDA product code for CATHETER VALVES KV 100 & KV 100EH is KOD.

Related Clinical Trials

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.

Related Devices (Code: KOD)

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.

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.

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