Weaver & Co.
Country not established
- Devices
- 3
What Weaver & Co. makes
Weaver & Co. manufactures medical preparation kits, including OMNIPREP and NUPREP, designed for patient skin preparation prior to surgical procedures. The company also produces the PT-100-30 somatosensory stimulating electrode, a device used for nerve stimulation therapy.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. Weaver & Co. is based in the United States.
Catalogue
Omniprep Ref K781989
Regimes: 510(k) Registry: 510(k)Nuprep Ref K885306
Regimes: 510(k) Registry: 510(k)Pt-100-30 Somatosensory Stimulating Electrode Ref K874075
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Weaver & Co. have in the registry?
The registry currently lists 3 devices for Weaver & Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weaver & Co.'s devices?
Among its 3 most recently registered devices, Weaver & Co. has devices listed in FDA 510(k) (3 devices).
What risk classes do Weaver & Co.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Weaver & Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Weaver & Co. in the registry?
The most recently registered devices listed for Weaver & Co. include OMNIPREP, NUPREP and PT-100-30 SOMATOSENSORY STIMULATING ELECTRODE.