MODIFICATION TO EZ HUBER SAFETY INFUSION SET
K-Number: K071846 · 2007-08-30
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO EZ HUBER SAFETY INFUSION SET?
MODIFICATION TO EZ HUBER SAFETY INFUSION SET is a medical device that received FDA 510(k) clearance on 2007-08-30. The listed applicant is Pfm Medical, Inc.. The 510(k) number is K071846.
When did MODIFICATION TO EZ HUBER SAFETY INFUSION SET receive FDA 510(k) clearance?
MODIFICATION TO EZ HUBER SAFETY INFUSION SET received FDA 510(k) clearance on 2007-08-30, under 510(k) number K071846.
Who is the listed applicant for MODIFICATION TO EZ HUBER SAFETY INFUSION SET?
The FDA 510(k) record lists Pfm Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO EZ HUBER SAFETY INFUSION SET?
The FDA product code for MODIFICATION TO EZ HUBER 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.
Other records listing Pfm Medical, Inc. 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.
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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