Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Rocap Div. of Sabratek Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K990390	HEPARIN IV FLUSH SYRINGE, 10 U/ML \	FOZ	1999-12-10	View
510(k)	K990308	ROCAP HEPARIN IV FLUSH SYRINGE, 100U/ML	FOZ	1999-12-10	View
510(k)	K984614	NORMAL SALINE FLUSH SYRINGE	FOZ	1999-05-27	View

↑