MINILOC SAFETY INFUSION SET
K-Number: K050600 · 2005-05-12
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Device Summary
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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