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FDA 510(k)

VOYAGER PERITONEAL DIALYSIS SYSTEM

K-Number: K103220 · 2011-07-29

Decision Date2011-07-29
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VOYAGER PERITONEAL DIALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Deka Research & Development Corp.. It received FDA 510(k) clearance on 2011-07-29 under 510(k) number K103220. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOYAGER PERITONEAL DIALYSIS SYSTEM?

VOYAGER PERITONEAL DIALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 2011-07-29. The listed applicant is Deka Research & Development Corp.. The 510(k) number is K103220.

When did VOYAGER PERITONEAL DIALYSIS SYSTEM receive FDA 510(k) clearance?

VOYAGER PERITONEAL DIALYSIS SYSTEM received FDA 510(k) clearance on 2011-07-29, under 510(k) number K103220.

Who is the listed applicant for VOYAGER PERITONEAL DIALYSIS SYSTEM?

The FDA 510(k) record lists Deka Research & Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOYAGER PERITONEAL DIALYSIS SYSTEM?

The FDA product code for VOYAGER PERITONEAL DIALYSIS SYSTEM is FKX.

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 Deka Research & Development Corp. 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 11 devices →

Related Devices (Code: FKX)

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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