Medical Device Manufacturer · US , Orlando , FL

Rocap Div. of Sabratek Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1999

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rocap Div. of Sabratek Corp. General Hospital ✕

3 devices

1-3 of 3

Cleared Dec 10, 1999

ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML

General Hospital · 312d

Cleared Dec 10, 1999

HEPARIN IV FLUSH SYRINGE, 10 U/ML \

General Hospital · 304d

Cleared May 27, 1999

NORMAL SALINE FLUSH SYRINGE

General Hospital · 149d