Rocap Div. of Sabratek Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Rocap Div. of Sabratek Corp. makes
Rocap Div. of Sabratek Corp. manufactures pre-filled saline and heparin flush syringes for intravenous use, including normal saline flush syringes and heparin flush syringes in 10 U/mL and 100 U/mL concentrations.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Normal Saline Flush Syringe Ref K984614
Regimes: 510(k) Registry: 510(k)Rocap Heparin Iv Flush Syringe, 100U/Ml Ref K990308
Regimes: 510(k) Registry: 510(k)Heparin Iv Flush Syringe, 10 U/Ml \ Ref K990390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rocap Div. of Sabratek Corp. have in the registry?
The registry currently lists 3 devices for Rocap Div. of Sabratek Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rocap Div. of Sabratek Corp.'s devices?
Among its 3 most recently registered devices, Rocap Div. of Sabratek Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rocap Div. of Sabratek Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rocap Div. of Sabratek Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rocap Div. of Sabratek Corp. in the registry?
The most recently registered devices listed for Rocap Div. of Sabratek Corp. include NORMAL SALINE FLUSH SYRINGE, ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML and HEPARIN IV FLUSH SYRINGE, 10 U/ML \.