Micro-Tech Diagnostic, Inc.
Country not established
- Devices
- 1
What Micro-Tech Diagnostic, Inc. makes
Micro-Tech Diagnostic, Inc. manufactures the Improved Thayer-Martin Medium, a selective culture medium used for isolating *Neisseria gonorrhoeae* and *Neisseria meningitidis* from clinical specimens.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The product is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Improved Thayer-Martin Medium Ref K770925
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micro-Tech Diagnostic, Inc. have in the registry?
The registry currently lists 1 device for Micro-Tech Diagnostic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro-Tech Diagnostic, Inc.'s devices?
Among its 1 most recently registered device, Micro-Tech Diagnostic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Micro-Tech Diagnostic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Micro-Tech Diagnostic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micro-Tech Diagnostic, Inc. in the registry?
The most recently registered devices listed for Micro-Tech Diagnostic, Inc. include IMPROVED THAYER-MARTIN MEDIUM.