Artel, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Artel, Inc. makes
Artel, Inc. manufactures photometric instruments for clinical and research use, including differential photometers for measuring light absorption, hemoglobinometers for quantifying hemoglobin levels, and single-wavelength mini photometers for specialized optical analysis.
The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. These instruments are listed in the FDA’s 510(k) clearance registry and are based in the United States.
Catalogue
Artel Differential Photometer Ref K864542
Regimes: 510(k) Registry: 510(k)Hbm Hemoglobinometer Ref K933836
Regimes: 510(k) Registry: 510(k)Mp/S Single Wavelength Mini Photometer Ref K920914
Regimes: 510(k) Registry: 510(k)Mp Mini Photometer Ref K914809
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artel, Inc. have in the registry?
The registry currently lists 4 devices for Artel, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artel, Inc.'s devices?
Among its 4 most recently registered devices, Artel, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Artel, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Artel, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artel, Inc. in the registry?
The most recently registered devices listed for Artel, Inc. include ARTEL DIFFERENTIAL PHOTOMETER, HBM HEMOGLOBINOMETER, MP/S SINGLE WAVELENGTH MINI PHOTOMETER and MP MINI PHOTOMETER.