Craig & Craig, Inc.
Country not established
- Devices
- 1
What Craig & Craig, Inc. makes
Craig & Craig, Inc. manufactures the Myowire, a temporary cardiac pacing wire designed for short-term pacing support in clinical settings.
The Myowire is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Myowire-Atemporary Cardiac Pacing Wire Ref K803086
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Craig & Craig, Inc. have in the registry?
The registry currently lists 1 device for Craig & Craig, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Craig & Craig, Inc.'s devices?
Among its 1 most recently registered device, Craig & Craig, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Craig & Craig, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Craig & Craig, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Craig & Craig, Inc. in the registry?
The most recently registered devices listed for Craig & Craig, Inc. include MYOWIRE-ATEMPORARY CARDIAC PACING WIRE.