POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS— 510(k) K100432

Substantially Equivalent

Medtronic Minimed

FDA 510(k) clearance K100432 for POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS, Substantially Equivalent on 2010-07-09. Applicant: Medtronic Minimed.

Clearance details

Applicant: Medtronic Minimed
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2010-02-16
Decision date: 2010-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northridge, CA, US

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Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.