SOF-SET MICRO QR INFUSION SET, MODELS 320 AND 321
K-Number: K991979 · 1999-09-03
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Device Summary
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.
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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