Sunscope Intl., Inc.
Sunscope Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2000.
Top product codes for Sunscope Intl., Inc.
Recent clearances by Sunscope Intl., Inc.
- K002786 — BIOSENSORS CENTRAL VENOUS CATHETER KITS
- K983372 — BIOPORT CLOSED BLOOD SAMPLING SYSTEM, MODEL BT XXXXXX- BP
- K973477 — BIOSENSORS EMBOLECTOMY CATHETER
- K981747 — BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX
- K981745 — BIOTRANS REUSABLE SENSOR BASE MODEL NUMBER BT XXXXXX
- K911710 — HEPARIN COATED THERMODILUTION CATH & ACCESSORIES
- K912172 — SAFEWEDGE(TM) RELIEF VALVE DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.