Medcor, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lithicron Ii 0403 Implantable Pacemaker Ref K791678
Regimes: 510(k) Registry: 510(k)Lithicron Model 3-70C-B Pulse Generator Ref K771538
Regimes: 510(k) Registry: 510(k)Lithicron 0520 P-Synchroneous Pulse Gen. Ref K792609
Regimes: 510(k) Registry: 510(k)Lithicron Model 0401, Pacemaker Ref K791095
Regimes: 510(k) Registry: 510(k)Lithicron F Programmable Pulse Gen Ref K780430
Regimes: 510(k) Registry: 510(k)Quintrex 0516 Prog. Pulse Generator Sys Ref K802224
Regimes: 510(k) Registry: 510(k)Pulse Generator, Litkicron Model 3-70H Ref K770507
Regimes: 510(k) Registry: 510(k)Quintrex 0515 Programmable Pulse Gen. Ref K802223
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medcor, Inc. have in the registry?
The registry currently lists 8 devices for Medcor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcor, Inc.'s devices?
Among its 8 most recently registered devices, Medcor, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Medcor, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Medcor, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Medcor, Inc. in the registry?
The most recently registered devices listed for Medcor, Inc. include LITHICRON II 0403 IMPLANTABLE PACEMAKER, LITHICRON MODEL 3-70C-B PULSE GENERATOR, LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN. and LITHICRON MODEL 0401, PACEMAKER.