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FDA 510(k)

HUBERPRO SAFETY HUBER INFUSION SET

K-Number: K033515 · 2004-01-22

Decision Date2004-01-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HUBERPRO SAFETY HUBER INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Command Medical Products. It received FDA 510(k) clearance on 2004-01-22 under 510(k) number K033515. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUBERPRO SAFETY HUBER INFUSION SET?

HUBERPRO SAFETY HUBER INFUSION SET is a medical device that received FDA 510(k) clearance on 2004-01-22. The listed applicant is Command Medical Products. The 510(k) number is K033515.

When did HUBERPRO SAFETY HUBER INFUSION SET receive FDA 510(k) clearance?

HUBERPRO SAFETY HUBER INFUSION SET received FDA 510(k) clearance on 2004-01-22, under 510(k) number K033515.

Who is the listed applicant for HUBERPRO SAFETY HUBER INFUSION SET?

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

What is the FDA product code for HUBERPRO SAFETY HUBER INFUSION SET?

The FDA product code for HUBERPRO SAFETY HUBER INFUSION SET is FPA.

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.

Related Devices (Code: FPA)

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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