Panatrex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Panatrex, Inc. makes
Panatrex, Inc. manufactures the QUANTI-TEST SYSTEM, a diagnostic device used for quantitative analysis in medical testing, and a range of vaginal specula (VAG O SPECULUM, Models VS1, VM1, VL1) designed for gynecological examinations.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. Panatrex, Inc. is based in the United States.
Catalogue
Quanti-Test System Ref K982578
Regimes: 510(k) Registry: 510(k)Vag O Speculum, Models VS1, VM1, VL1 Ref K042950
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Panatrex, Inc. have in the registry?
The registry currently lists 2 devices for Panatrex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Panatrex, Inc.'s devices?
Among its 2 most recently registered devices, Panatrex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Panatrex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Panatrex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Panatrex, Inc. in the registry?
The most recently registered devices listed for Panatrex, Inc. include QUANTI-TEST SYSTEM and VAG O SPECULUM, MODELS VS1, VM1, VL1.