Tudor Laboratories, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
Catalogue
Digitoxin (Fpia) Kit Ref K913240
510(k) 510(k)Primidone (Fpia) Calibrator Kit Ref K895568
510(k) 510(k)N-Acetylprocainamide (Napa) Calibrator Kit Ref K895572
510(k) 510(k)Valproic Acid (Fpia) Calibrator Kit Ref K895570
510(k) 510(k)Thyroxine (Fpia) Kit Ref K921904
510(k) 510(k)Valproic Acid (Fpia) Kit Ref K895569
510(k) 510(k)Thyroxine Calibrator Kit Ref K921903
510(k) 510(k)Primidone (Fpia) Kit Ref K895567
510(k) 510(k)N-Acetylprocainamide (Napa) (Fpia) Kit Ref K895571
510(k) 510(k)
Frequently asked questions
How many devices does Tudor Laboratories, Inc. have in the registry?
The registry currently lists 9 devices for Tudor Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tudor Laboratories, Inc.'s devices?
Among its 9 most recently registered devices, Tudor Laboratories, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Tudor Laboratories, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Tudor Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tudor Laboratories, Inc. in the registry?
The most recently registered devices listed for Tudor Laboratories, Inc. include DIGITOXIN (FPIA) KIT, PRIMIDONE (FPIA) CALIBRATOR KIT, N-ACETYLPROCAINAMIDE (NAPA) CALIBRATOR KIT and VALPROIC ACID (FPIA) CALIBRATOR KIT.