Bug City Company, Inc.
Country not established
- Devices
- 1
What Bug City Company, Inc. makes
Bug City Company, Inc. manufactures the Chamber V-9 Plus Agar, a microbiological culture medium designed for isolating and identifying bacterial and fungal pathogens in clinical and research settings. This product is intended for use in microbiology laboratories to support diagnostic testing and quality control procedures.
The Chamber V-9 Plus Agar is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company operates from the United States, where its products are subject to compliance with the Federal Food, Drug, and Cosmetic Act.
Catalogue
Chamber V-9 Plus Agar Ref K851238
510(k) 510(k)
Frequently asked questions
How many devices does Bug City Company, Inc. have in the registry?
The registry currently lists 1 device for Bug City Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bug City Company, Inc.'s devices?
Among its 1 most recently registered device, Bug City Company, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bug City Company, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bug City Company, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bug City Company, Inc. in the registry?
The most recently registered devices listed for Bug City Company, Inc. include CHAMBER V-9 PLUS AGAR.