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FDA 510(k)

SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321

K-Number: K991979 · 1999-09-03

Decision Date1999-09-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K991979. 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 SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321?

SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Medtronic Minimed. The 510(k) number is K991979.

When did SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 receive FDA 510(k) clearance?

SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 received FDA 510(k) clearance on 1999-09-03, under 510(k) number K991979.

Who is the listed applicant for SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321?

The FDA 510(k) record lists Medtronic Minimed as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321?

The FDA product code for SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321 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 Medtronic Minimed 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 49 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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