Dr. Novis Smith & Co., Inc.
Country not established
- Devices
- 1
What Dr. Novis Smith & Co., Inc. makes
Dr. Novis Smith & Co., Inc. manufactures the NOVIGUARD QUICK DRY, a Class I medical device designed for rapid drying applications in healthcare settings.
The NOVIGUARD QUICK DRY is regulated under the FDA’s 510(k) pathway and is listed in the U.S. as a Class I device. The company is based in the United States.
Catalogue
Noviguard Quick Dry Ref K961044
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dr. Novis Smith & Co., Inc. have in the registry?
The registry currently lists 1 device for Dr. Novis Smith & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Novis Smith & Co., Inc.'s devices?
Among its 1 most recently registered device, Dr. Novis Smith & Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Novis Smith & Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Novis Smith & Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Novis Smith & Co., Inc. in the registry?
The most recently registered devices listed for Dr. Novis Smith & Co., Inc. include NOVIGUARD QUICK DRY.