REVERSE CURVE ARCHWIRE— 510(k) K880882
Substantially EquivalentFlexmedics
FDA 510(k) clearance K880882 for REVERSE CURVE ARCHWIRE, Substantially Equivalent on 1988-04-11. Applicant: Flexmedics. Device class: 1.
Clearance details
- Applicant
- Flexmedics
- Product code
- Code EJF
- 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 EJF
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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.