Urol, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Urol, Inc. makes
Urol, Inc. manufactures a specimen collection device for medical use, as well as a Bacillus pumilus reference material used in microbial challenge testing for device sterilisation validation.
The company’s products are classified under FDA Class I devices and are listed via 510(k) clearance in the United States. The company is headquartered in the US.
Catalogue
Bacillus Pumilus Ref K780974
Regimes: 510(k) Registry: 510(k)Specimen Collection Device Ref K780049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Urol, Inc. have in the registry?
The registry currently lists 2 devices for Urol, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Urol, Inc.'s devices?
Among its 2 most recently registered devices, Urol, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Urol, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Urol, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Urol, Inc. in the registry?
The most recently registered devices listed for Urol, Inc. include BACILLUS PUMILUS and SPECIMEN COLLECTION DEVICE.