MEDTRONIC ARTERIAL FILTER— 510(k) K926413
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K926413 for MEDTRONIC ARTERIAL FILTER, Substantially Equivalent on 1993-08-24. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code DTM
- Device class
- Class 2
- Regulation
- 21 CFR 870.4260
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Anaheim, CA, US
Recent devices under product code DTM
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- K220773 — Everest 20 Inflation Device and 3-way Stopcock (AC2200) +3 more
- K192296 — Medtronic 6F Taiga Guiding Catheter
Data sourced from openFDA. This site is unofficial and independent of the FDA.