MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313
K-Number: K032485 · 2003-10-28
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Device Summary
Frequently Asked Questions
What is the MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313?
MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313 is a medical device that received FDA 510(k) clearance on 2003-10-28. The listed applicant is Medtronic Minimed. The 510(k) number is K032485.
When did MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313 receive FDA 510(k) clearance?
MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313 received FDA 510(k) clearance on 2003-10-28, under 510(k) number K032485.
Who is the listed applicant for MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313?
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 MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313?
The FDA product code for MEDTRONIC MINIMED COUNTACH INFUSION SET, MODEL 313 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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