IMPLANTABLE PULSE GENERATORS— 510(k) K925106
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K925106 for IMPLANTABLE PULSE GENERATORS, Substantially Equivalent on 1993-10-06. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code DYX
- Device class
- Class 2
- Regulation
- 21 CFR 872.4600
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Recent devices under product code DYX
view allMore clearances from Medtronic Vascular
view all- K232570 — Steerant Super Stiff Guidewire
- K232190 — 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter
- K230156 — 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
- 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.