Cormed, Inc., Sub. C.R.Bard, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cormed Ii Ambulatory Infusion Pump Ref K850674
Regimes: 510(k) Registry: 510(k)Sterile Cormed Mediport Ref K850967
Regimes: 510(k) Registry: 510(k)Butterfly Non-Coring Needle Set Ref K863606
Regimes: 510(k) Registry: 510(k)Corcath H & B Vascular Access Catheter Ref K823553
Regimes: 510(k) Registry: 510(k)Port-Gard Ref K854019
Regimes: 510(k) Registry: 510(k)Cormed Huber Point Needle Ref K843083
Regimes: 510(k) Registry: 510(k)Percutaneous Introducer Kit Ref K860432
Regimes: 510(k) Registry: 510(k)Vascular Access Cath. Repair Kit Ref K833915
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cormed, Inc., Sub. C.R.Bard, Inc. have in the registry?
The registry currently lists 8 devices for Cormed, Inc., Sub. C.R.Bard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cormed, Inc., Sub. C.R.Bard, Inc.'s devices?
Among its 8 most recently registered devices, Cormed, Inc., Sub. C.R.Bard, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Cormed, Inc., Sub. C.R.Bard, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Cormed, Inc., Sub. C.R.Bard, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cormed, Inc., Sub. C.R.Bard, Inc. in the registry?
The most recently registered devices listed for Cormed, Inc., Sub. C.R.Bard, Inc. include CORMED II AMBULATORY INFUSION PUMP, STERILE CORMED MEDIPORT, BUTTERFLY NON-CORING NEEDLE SET and CORCATH H & B VASCULAR ACCESS CATHETER.