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FDA 510(k)

CENTROS CHRONIC HEMODIALYSIS CATHETER SET

K-Number: K092597 · 2009-11-12

Decision Date2009-11-12
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

CENTROS CHRONIC HEMODIALYSIS CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Ash Access Technology, Inc.. It received FDA 510(k) clearance on 2009-11-12 under 510(k) number K092597. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CENTROS CHRONIC HEMODIALYSIS CATHETER SET?

CENTROS CHRONIC HEMODIALYSIS CATHETER SET is a medical device that received FDA 510(k) clearance on 2009-11-12. The listed applicant is Ash Access Technology, Inc.. The 510(k) number is K092597.

When did CENTROS CHRONIC HEMODIALYSIS CATHETER SET receive FDA 510(k) clearance?

CENTROS CHRONIC HEMODIALYSIS CATHETER SET received FDA 510(k) clearance on 2009-11-12, under 510(k) number K092597.

Who is the listed applicant for CENTROS CHRONIC HEMODIALYSIS CATHETER SET?

The FDA 510(k) record lists Ash Access Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTROS CHRONIC HEMODIALYSIS CATHETER SET?

The FDA product code for CENTROS CHRONIC HEMODIALYSIS CATHETER SET 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.

Other records listing Ash Access Technology, 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: 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.

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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