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FDA 510(k)

HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR

K-Number: K050952 · 2006-01-31

Decision Date2006-01-31
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Minntech Corp.. It received FDA 510(k) clearance on 2006-01-31 under 510(k) number K050952. 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 HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR?

HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR is a medical device that received FDA 510(k) clearance on 2006-01-31. The listed applicant is Minntech Corp.. The 510(k) number is K050952.

When did HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR receive FDA 510(k) clearance?

HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR received FDA 510(k) clearance on 2006-01-31, under 510(k) number K050952.

Who is the listed applicant for HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR?

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

What is the FDA product code for HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR?

The FDA product code for HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATOR 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 Minntech 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 33 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

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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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