HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR— 510(k) K043080
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K043080 for HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR, Substantially Equivalent on 2004-12-03. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code JOX
- Device class
- Class 2
- Regulation
- 21 CFR 864.5680
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Minneapolis, MN, US
Recent devices under product code JOX
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.