Pancretec, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Provider Bag Spike W/12 Microbore Exten Ref K843463
Regimes: 510(k) Registry: 510(k)Provider U-100 Insulin Infusion Sys Ref K833983
Regimes: 510(k) Registry: 510(k)Provider Iv. Model 5000 Infusion Device Ref K871806
Regimes: 510(k) Registry: 510(k)Provider Pa 3000 Infusion System Ref K844078
Regimes: 510(k) Registry: 510(k)Provider Infusion Set Ref K841017
Regimes: 510(k) Registry: 510(k)Provider Iv Model 2000 Infusin Sys Ref K841373
Regimes: 510(k) Registry: 510(k)Provider Cap Set Ref K841028
Regimes: 510(k) Registry: 510(k)Provider One Infusion System Ref K882102
Regimes: 510(k) Registry: 510(k)Pancretec Pump Check Ref K841018
Regimes: 510(k) Registry: 510(k)Provider Site Prep & Check Strip Kit Ref K841027
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pancretec, Inc. have in the registry?
The registry currently lists 10 devices for Pancretec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pancretec, Inc.'s devices?
Among its 10 most recently registered devices, Pancretec, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Pancretec, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Pancretec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pancretec, Inc. in the registry?
The most recently registered devices listed for Pancretec, Inc. include PROVIDER BAG SPIKE W/12 MICROBORE EXTEN, PROVIDER U-100 INSULIN INFUSION SYS, PROVIDER IV. MODEL 5000 INFUSION DEVICE and PROVIDER PA 3000 INFUSION SYSTEM.