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FDA 510(k)

HEMOCATH II

K-Number: K062901 · 2007-02-08

ApplicantMed-Conduit, Inc.
Decision Date2007-02-08
Product CodeMSD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HEMOCATH II is the device name listed in this FDA 510(k) record. The listed applicant is Med-Conduit, Inc.. It received FDA 510(k) clearance on 2007-02-08 under 510(k) number K062901. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOCATH II?

HEMOCATH II is a medical device that received FDA 510(k) clearance on 2007-02-08. The listed applicant is Med-Conduit, Inc.. The 510(k) number is K062901.

When did HEMOCATH II receive FDA 510(k) clearance?

HEMOCATH II received FDA 510(k) clearance on 2007-02-08, under 510(k) number K062901.

Who is the listed applicant for HEMOCATH II?

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

What is the FDA product code for HEMOCATH II?

The FDA product code for HEMOCATH II is MSD.

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.

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Other records listing Med-Conduit, Inc. as applicant

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.

K053123PD CATHK043292HEMOCATH

Related Devices (Code: MSD)

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.

K241581Hemodialysis CatheterHaolang Medical USA CorporationK210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, Inc.

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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