Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger - FDA 510(k) Clear...
1
Total
1
Cleared
0
Denied
Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hemo-Sanitas, Inc. C/O Greenberg Irwin & Weisinger
1 devices