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FDA 510(k)

PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS

K-Number: K070430 · 2007-04-04

Decision Date2007-04-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PARADIGM QUICK-SET II AND QUICK-SET II SUBCUTANEOUS INFUSION SETS is the device name listed in this FDA 510(k) record. The listed applicant is Unomedical A/S. It received FDA 510(k) clearance on 2007-04-04 under 510(k) number K070430. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 13 devices →

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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