Spartan Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Spartan Laboratories, Inc. makes
Spartan Laboratories, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the Model SPL 2000 and SPL 2000S, designed for pain management through low-voltage electrical pulses.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
T.E.N.S. Device Model Spl 2000 Ref K872398
Regimes: 510(k) Registry: 510(k)T.E.N.S. Device Model Spl 2000S Ref K872399
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spartan Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for Spartan Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spartan Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, Spartan Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Spartan Laboratories, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Spartan Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spartan Laboratories, Inc. in the registry?
The most recently registered devices listed for Spartan Laboratories, Inc. include T.E.N.S. DEVICE MODEL SPL 2000 and T.E.N.S. DEVICE MODEL SPL 2000S.