Tek Marketing, Inc.
Country not established
- Devices
- 1
What Tek Marketing, Inc. makes
Tek Marketing, Inc. manufactures the MICRO-MAX, Model 319, a medical device designed for a specific clinical application (device category not specified in data).
The MICRO-MAX, Model 319 is classified as a Class II device under FDA regulations and is supported by a 510(k) clearance. The company is based in the United States.
Catalogue
Micro-Max, Model 319 Ref K002404
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tek Marketing, Inc. have in the registry?
The registry currently lists 1 device for Tek Marketing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tek Marketing, Inc.'s devices?
Among its 1 most recently registered device, Tek Marketing, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tek Marketing, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tek Marketing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tek Marketing, Inc. in the registry?
The most recently registered devices listed for Tek Marketing, Inc. include MICRO-MAX, MODEL 319.