FLEXMEDICS NITINOL ARCH WIRE— 510(k) K863742
Substantially EquivalentFlexmedics
FDA 510(k) clearance K863742 for FLEXMEDICS NITINOL ARCH WIRE, Substantially Equivalent on 1986-11-24. Applicant: Flexmedics. Device class: 1.
Clearance details
- Applicant
- Flexmedics
- Product code
- Code DZC
- Device class
- Class 1
- Regulation
- 21 CFR 872.5410
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
Recent devices under product code DZC
view allMore clearances from Flexmedics
view all- K990765 — FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO
- K964955 — FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKING
- K952430 — FINESSE GUIDEWIRE CORONARY
- K943390 — FLEXFINDER GUIDEWIRE
- K942074 — FLEXFINDER GUIDEWIRE
Data sourced from openFDA. This site is unofficial and independent of the FDA.