Palco Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Palco Labs Model 300 Oxygen/Pulse Monitor Ref K911191
Regimes: 510(k) Registry: 510(k)Wet-Stop Ref K842547
Regimes: 510(k) Registry: 510(k)Auto-Lancet Ref K833344
Regimes: 510(k) Registry: 510(k)Palco Labs Cold Pouch Ref K942810
Regimes: 510(k) Registry: 510(k)Palco Labs Model 340 Pulse Oximeter Ref K920066
Regimes: 510(k) Registry: 510(k)Pulse Oximeter Model 305 Ref K943842
Regimes: 510(k) Registry: 510(k)Palco Labs Model 400 Oxygen/Pulse Monitor Ref K904988
Regimes: 510(k) Registry: 510(k)Inject-Ease Ref K872233
Regimes: 510(k) Registry: 510(k)Palco Labs Loadmatic Ref K913694
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Palco Laboratories, Inc. have in the registry?
The registry currently lists 9 devices for Palco Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Palco Laboratories, Inc.'s devices?
Among its 9 most recently registered devices, Palco Laboratories, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Palco Laboratories, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Palco Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Palco Laboratories, Inc. in the registry?
The most recently registered devices listed for Palco Laboratories, Inc. include PALCO LABS MODEL 300 OXYGEN/PULSE MONITOR, WET-STOP, AUTO-LANCET and PALCO LABS COLD POUCH.