Electro-Spec, Inc.
Country not established
- Devices
- 1
What Electro-Spec, Inc. makes
Electro-Spec, Inc. manufactures Electro-Spec Steri-Caps, a sterile barrier device designed for single-use electrical connector applications in medical equipment to prevent contamination during use.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
Electro-Spec Steri-Caps Ref K231905
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electro-Spec, Inc. have in the registry?
The registry currently lists 1 device for Electro-Spec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electro-Spec, Inc.'s devices?
Among its 1 most recently registered device, Electro-Spec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Electro-Spec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Electro-Spec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electro-Spec, Inc. in the registry?
The most recently registered devices listed for Electro-Spec, Inc. include Electro-Spec Steri-Caps.