Labarge, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Labarge, Inc. makes
Labarge, Inc. manufactures esophageal stethoscopes, non-auditory stethoscopes, esophageal stethoscope temperature sensors, and a monothermal temperature monitoring system for medical use.
These devices are regulated under FDA 510(k) clearance, with classifications including Class I and Class II. The company is based in the United States.
Catalogue
Esophageal Stethoscope Ref K771520
Regimes: 510(k) Registry: 510(k)Non-A-Therm Ref K792037
Regimes: 510(k) Registry: 510(k)Esophageal Steth. Temp. Sensor Ref K771411
Regimes: 510(k) Registry: 510(k)Mon-A-Therm Temparature Monitor Sys Ref K760720
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Labarge, Inc. have in the registry?
The registry currently lists 4 devices for Labarge, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Labarge, Inc.'s devices?
Among its 4 most recently registered devices, Labarge, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Labarge, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Labarge, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Labarge, Inc. in the registry?
The most recently registered devices listed for Labarge, Inc. include ESOPHAGEAL STETHOSCOPE, NON-A-THERM, ESOPHAGEAL STETH. TEMP. SENSOR and MON-A-THERM TEMPARATURE MONITOR SYS.