SUREFLOW SAFETY INFUSION DEVICE
K-Number: K051943 · 2005-10-04
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Device Summary
Frequently Asked Questions
What is the SUREFLOW SAFETY INFUSION DEVICE?
SUREFLOW SAFETY INFUSION DEVICE is a medical device that received FDA 510(k) clearance on 2005-10-04. The listed applicant is Intrasafe Medical, LLC. The 510(k) number is K051943.
When did SUREFLOW SAFETY INFUSION DEVICE receive FDA 510(k) clearance?
SUREFLOW SAFETY INFUSION DEVICE received FDA 510(k) clearance on 2005-10-04, under 510(k) number K051943.
Who is the listed applicant for SUREFLOW SAFETY INFUSION DEVICE?
The FDA 510(k) record lists Intrasafe Medical, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUREFLOW SAFETY INFUSION DEVICE?
The FDA product code for SUREFLOW SAFETY INFUSION DEVICE 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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