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FDA 510(k)

MINILOC SAFETY INFUSION SET

K-Number: K050600 · 2005-05-12

Decision Date2005-05-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MINILOC SAFETY INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Specialized Health Products, Intl.. It received FDA 510(k) clearance on 2005-05-12 under 510(k) number K050600. 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 MINILOC SAFETY INFUSION SET?

MINILOC SAFETY INFUSION SET is a medical device that received FDA 510(k) clearance on 2005-05-12. The listed applicant is Specialized Health Products, Intl.. The 510(k) number is K050600.

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

MINILOC SAFETY INFUSION SET received FDA 510(k) clearance on 2005-05-12, under 510(k) number K050600.

Who is the listed applicant for MINILOC SAFETY INFUSION SET?

The FDA 510(k) record lists Specialized Health Products, Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINILOC SAFETY INFUSION SET?

The FDA product code for MINILOC SAFETY 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

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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