PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS
K-Number: K070430 · 2007-04-04
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Device Summary
Frequently Asked Questions
What is the PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS?
PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS is a medical device that received FDA 510(k) clearance on 2007-04-04. The listed applicant is Unomedical A/S. The 510(k) number is K070430.
When did PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS receive FDA 510(k) clearance?
PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS received FDA 510(k) clearance on 2007-04-04, under 510(k) number K070430.
Who is the listed applicant for PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS 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 PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS?
The FDA product code for PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS 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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