UNOMEDICAL MONICA INFUSION SET
K-Number: K032854 · 2003-10-09
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Device Summary
Frequently Asked Questions
What is the UNOMEDICAL MONICA INFUSION SET?
UNOMEDICAL MONICA INFUSION SET is a medical device that received FDA 510(k) clearance on 2003-10-09. The listed applicant is Unomedical A/S. The 510(k) number is K032854.
When did UNOMEDICAL MONICA INFUSION SET receive FDA 510(k) clearance?
UNOMEDICAL MONICA INFUSION SET received FDA 510(k) clearance on 2003-10-09, under 510(k) number K032854.
Who is the listed applicant for UNOMEDICAL MONICA INFUSION SET?
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 UNOMEDICAL MONICA INFUSION SET?
The FDA product code for UNOMEDICAL MONICA 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 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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