Konica Minolta Sensing, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Konica Minolta Sensing, Inc. makes
The company manufactures pulse oximeters, including models such as the MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI, KONICA MINOLTA PULSOX-300, 300I, and MINOLTA PULSOX-2. These devices are designed for non-invasive monitoring of blood oxygen saturation (SpO₂) and pulse rate, commonly used in clinical and home healthcare settings.
The portfolio consists of Class II medical devices, each authorised through the FDA’s 510(k) clearance process. These products are listed under the US regulatory framework and are intended for use in the United States.
Catalogue
Minolta Pulsox-3SI, Pulsox-3IA, Pulsox-3LI Ref K010413
510(k) 510(k)Konica Minolta Pulsox-300, 300I Ref K053419
510(k) 510(k)Minolta Pulsox-2 Ref K021469
510(k) 510(k)
Frequently asked questions
How many devices does Konica Minolta Sensing, Inc. have in the registry?
The registry currently lists 3 devices for Konica Minolta Sensing, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Konica Minolta Sensing, Inc.'s devices?
Among its 3 most recently registered devices, Konica Minolta Sensing, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Konica Minolta Sensing, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Konica Minolta Sensing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Konica Minolta Sensing, Inc. in the registry?
The most recently registered devices listed for Konica Minolta Sensing, Inc. include MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI, KONICA MINOLTA PULSOX-300, 300I and MINOLTA PULSOX-2.