Altech® Exhalation Valve (Single Limb and Dual Limb)— 510(k) K210992
Substantially EquivalentMeditera Tibbi Malzeme San VE Tic AS
FDA 510(k) clearance K210992 for Altech® Exhalation Valve (Single Limb and Dual Limb), Substantially Equivalent on 2021-12-23. Applicant: Meditera Tibbi Malzeme San VE Tic AS. Device class: 2.
Clearance details
- Applicant
- Meditera Tibbi Malzeme San VE Tic AS
- Product code
- Code CBP
- Device class
- Class 2
- Regulation
- 21 CFR 868.5870
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tire Izmir, TR
Recent devices under product code CBP
view all- K241366 — QualityFlow O2 Series (QualityFLOW O2); QualityFlow O2 Series (QualityFLOW O2 MTV)
- K234053 — F&P Optiflow Flow Diverter
- K192285 — CPR Face Shield
- K173770 — OJR215 Pressure Relief Manifold
- K171961 — Compower CPR Mask With Oxygen Port, Compower CPR Mask Without Oxygen Port, Compower Infant CPR Mask, Compower Non-Rebreathing Valve (22mm/15mmOD), Non-Rebreathing Valve (22mm/18.5mm)
More clearances from Meditera Tibbi Malzeme San VE Tic AS
view allData sourced from openFDA. This site is unofficial and independent of the FDA.