INTUITION INFUSION SETS
K-Number: K061374 · 2006-07-31
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Device Summary
Frequently Asked Questions
What is the INTUITION INFUSION SETS?
INTUITION INFUSION SETS is a medical device that received FDA 510(k) clearance on 2006-07-31. The listed applicant is Unomedical A/S. The 510(k) number is K061374.
When did INTUITION INFUSION SETS receive FDA 510(k) clearance?
INTUITION INFUSION SETS received FDA 510(k) clearance on 2006-07-31, under 510(k) number K061374.
Who is the listed applicant for INTUITION INFUSION SETS?
The FDA 510(k) record lists Unomedical A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTUITION INFUSION SETS?
The FDA product code for INTUITION INFUSION SETS 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 Unomedical A/S 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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