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FDA 510(k)

FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM

K-Number: K890824 · 1989-05-11

ApplicantFresenius USA, Inc.
Decision Date1989-05-11
Product CodeFKP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius USA, Inc.. It received FDA 510(k) clearance on 1989-05-11 under 510(k) number K890824. The device is classified under product code FKP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM?

FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is Fresenius USA, Inc.. The 510(k) number is K890824.

When did FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM receive FDA 510(k) clearance?

FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM received FDA 510(k) clearance on 1989-05-11, under 510(k) number K890824.

Who is the listed applicant for FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM?

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

What is the FDA product code for FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM?

The FDA product code for FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM is FKP.

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Other records listing Fresenius USA, Inc. as applicant

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Related Devices (Code: FKP)

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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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