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FDA 510(k)

FRESENIUS 2008T HEMODIALYSIS MACHINE

K-Number: K113427 · 2011-12-21

Decision Date2011-12-21
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FRESENIUS 2008T HEMODIALYSIS MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Medical Care North America. It received FDA 510(k) clearance on 2011-12-21 under 510(k) number K113427. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRESENIUS 2008T HEMODIALYSIS MACHINE?

FRESENIUS 2008T HEMODIALYSIS MACHINE is a medical device that received FDA 510(k) clearance on 2011-12-21. The listed applicant is Fresenius Medical Care North America. The 510(k) number is K113427.

When did FRESENIUS 2008T HEMODIALYSIS MACHINE receive FDA 510(k) clearance?

FRESENIUS 2008T HEMODIALYSIS MACHINE received FDA 510(k) clearance on 2011-12-21, under 510(k) number K113427.

Who is the listed applicant for FRESENIUS 2008T HEMODIALYSIS MACHINE?

The FDA 510(k) record lists Fresenius Medical Care North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRESENIUS 2008T HEMODIALYSIS MACHINE?

The FDA product code for FRESENIUS 2008T HEMODIALYSIS MACHINE is KDI.

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 Fresenius Medical Care North America 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.

View all 40 devices →

Related Devices (Code: KDI)

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

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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