Mallinckroot, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Foley-Temp(Tm) Ref K882130
Regimes: 510(k) Registry: 510(k)A-V(Tm) Softouch Uhf Cardiac Pigtail Ref K885348
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Clear Shot Angioplasty Balloon Inflation Device Ref K884481
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Modified Softouch Introducer W/Hemo Valve & Side Ref K894445
Regimes: 510(k) Registry: 510(k)Attachable Lanz (Tentative) Ref K885216
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mallinckroot, Inc. have in the registry?
The registry currently lists 7 devices for Mallinckroot, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mallinckroot, Inc.'s devices?
Among its 7 most recently registered devices, Mallinckroot, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Mallinckroot, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Mallinckroot, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mallinckroot, Inc. in the registry?
The most recently registered devices listed for Mallinckroot, Inc. include FOLEY-TEMP(TM), A-V(TM) SOFTOUCH UHF CARDIAC PIGTAIL, COPPERHEAD 5 FR. PTA CATHETER, FINCH 4 FR. PTA CATHETER and CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE.