Capintec Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dose Calibrator Ref K905796
Regimes: 510(k) Registry: 510(k)Captus 500 Ref K921428
Regimes: 510(k) Registry: 510(k)Captus 2000 Wel Counter Ref K930962
Regimes: 510(k) Registry: 510(k)Capintec Thyroid Uptake System-Various Models Ref K910020
Regimes: 510(k) Registry: 510(k)Capintec Crc 35R Ref K935539
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Beta C Counter Ref K943072
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Capintec Instruments, Inc. have in the registry?
The registry currently lists 7 devices for Capintec Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Capintec Instruments, Inc.'s devices?
Among its 7 most recently registered devices, Capintec Instruments, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Capintec Instruments, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Capintec Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Capintec Instruments, Inc. in the registry?
The most recently registered devices listed for Capintec Instruments, Inc. include DOSE CALIBRATOR, CAPTUS 500, CAPTUS 2000 WEL COUNTER and CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS.