Midwest Rhino XE and Air Motor M
K-Number: K192409 · 2020-01-13
ApplicantDentsply Sirona
Decision Date2020-01-13
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Midwest Rhino XE and Air Motor M is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2020-01-13 under approval number K192409. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Midwest Rhino XE and Air Motor M?
Midwest Rhino XE and Air Motor M is a medical device that received FDA 510(k) clearance on 2020-01-13. It is manufactured by Dentsply Sirona. The 510(k) number is K192409.
When was Midwest Rhino XE and Air Motor M approved by the FDA?
Midwest Rhino XE and Air Motor M received FDA 510(k) clearance on 2020-01-13, under approval number K192409.
What company makes Midwest Rhino XE and Air Motor M?
Midwest Rhino XE and Air Motor M is manufactured by Dentsply Sirona.
What is the FDA product code for Midwest Rhino XE and Air Motor M?
The FDA product code for Midwest Rhino XE and Air Motor M is EFB.
Other Devices by Dentsply Sirona
Related Devices (Code: EFB)
K160410WOlf High Speed Handpieces - Medium head, WOlf High Speed Handpieces - Small headDental Savings Club
K153411430 Torque High-Speed Handpiece Series - 430 SWL Torque High Speed Handpiece, 430 SW Torque High Speed HandpieceDentalez, Inc.
K151912AIR-FLOW handy 3.0 PLUSE.M.S Electro Medical Systems S.A
K171174PERIO-FLOW nozzleE.M.S Electro Medical Systems S.A
K171553W&H Assistina TwinW&H Dentalwerk Buermoos GmbH
K170236Dental Low-speed Turbine HandpieceGuangdong Jinme Medical Technology Co., Ltd.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.