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FDA 510(k)

PD CATH

K-Number: K053123 · 2006-03-29

Decision Date2006-03-29
Product CodeFJS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PD CATH 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 2006-03-29 under 510(k) number K053123. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PD CATH?

PD CATH is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Med-Conduit, Inc.. The 510(k) number is K053123.

When did PD CATH receive FDA 510(k) clearance?

PD CATH received FDA 510(k) clearance on 2006-03-29, under 510(k) number K053123.

Who is the listed applicant for PD CATH?

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 PD CATH?

The FDA product code for PD CATH is FJS.

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.

Related Devices (Code: FJS)

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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