Medical Electronics Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medical Electronics Laboratories, Inc. makes
Medical Electronics Laboratories, Inc. manufactures patient monitoring devices, including the Siemens SireCust 1280 and 1281 with arrhythmia software, as well as the SireCust Model 960 and 961 for real-time patient vital sign tracking.
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
- Regimes: 510(k) Registry: 510(k)
Sirecust Model 960 And 961 Patient Monitoring Ref K872249
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Electronics Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for Medical Electronics Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Electronics Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, Medical Electronics Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medical Electronics Laboratories, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medical Electronics Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Electronics Laboratories, Inc. in the registry?
The most recently registered devices listed for Medical Electronics Laboratories, Inc. include SIEMENS SIRECUST 1280, 1281 W/ARRHYTHMIA SOFTWARE and SIRECUST MODEL 960 AND 961 PATIENT MONITORING.