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FDA 510(k)

DLC 500, DOUBLE LUMEN CATHETER

K-Number: K781050 · 1978-09-26

ApplicantHemodialysis, Division of The
Decision Date1978-09-26
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DLC 500, DOUBLE LUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Hemodialysis, Division of The. It received FDA 510(k) clearance on 1978-09-26 under 510(k) number K781050. 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 DLC 500, DOUBLE LUMEN CATHETER?

DLC 500, DOUBLE LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 1978-09-26. The listed applicant is Hemodialysis, Division of The. The 510(k) number is K781050.

When did DLC 500, DOUBLE LUMEN CATHETER receive FDA 510(k) clearance?

DLC 500, DOUBLE LUMEN CATHETER received FDA 510(k) clearance on 1978-09-26, under 510(k) number K781050.

Who is the listed applicant for DLC 500, DOUBLE LUMEN CATHETER?

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

What is the FDA product code for DLC 500, DOUBLE LUMEN CATHETER?

The FDA product code for DLC 500, DOUBLE LUMEN CATHETER is KOC.

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Related Devices (Code: KOC)

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.

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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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