Prepared Media Laboratory, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Prepared Media Laboratory, Inc. makes
Prepared Media Laboratory, Inc. manufactures microbiological culture media, including Enteric Pathogen Transport (EPT) systems for specimen collection and transport, Haemophilus Test Medium Agar for bacterial isolation, and Martin-Lewis Medium for selective fungal culture.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These media are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Enteric Pathogen Transport (Ept) (E1020, E1000) Ref K962745
Regimes: 510(k) Registry: 510(k)Haemophilus Test Medium Agar (Htm) Ref K962744
Regimes: 510(k) Registry: 510(k)Martin-Lewis Medium Ref K782117
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prepared Media Laboratory, Inc. have in the registry?
The registry currently lists 3 devices for Prepared Media Laboratory, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prepared Media Laboratory, Inc.'s devices?
Among its 3 most recently registered devices, Prepared Media Laboratory, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Prepared Media Laboratory, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Prepared Media Laboratory, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prepared Media Laboratory, Inc. in the registry?
The most recently registered devices listed for Prepared Media Laboratory, Inc. include ENTERIC PATHOGEN TRANSPORT (EPT) (E1020, E1000), HAEMOPHILUS TEST MEDIUM AGAR (HTM) and MARTIN-LEWIS MEDIUM.