Vertex Medical Corp.
Vertex Medical Corp. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1984.
Top product codes for Vertex Medical Corp.
Recent clearances by Vertex Medical Corp.
- K833742 — ESCHMANN DILATION CATHETER
- K834476 — NEPHROSTOMY/BILIARY DRAINAGE BAG
- K832380 — PROTECTIVE SLEEVE
- K831666 — SIALOGRAPHY NEEDLE
- K830576 — LYMPHANGIOGRAPHY SET
- K830420 — POLYETHYLENE MONITORING CONNECTORS
- K830237 — TRANSLUCENT POLY. CATH. CONNECTOR AND
- K823190 — BACKSTOP VALVE W/SIDE ARM
- K823191 — DISPOSABLE PLASTIC STOPCOCK
- K823192 — TUOHY-BORST ADAPTER W/SIDE ARM
- K823253 — VERTEX MONITORING CATHETER
- K823254 — REUSABLE METAL STOPCOCK
- K823256 — ULTRA-ASEPT ANGIOGRAPHIC SYRINGE/SPARE
- K823340 — CLEAR VINYL MONITORING CONNECTOR
- K823255 — NON-STERILE REUSABLE NEEDLES
- K822593 — PERCUTANEOUS CATHETER INTRODUCER SET
- K822594 — POLYETHYLENE CARDIOVASCULAR CATHETER
- K822595 — VESSEL DILATOR
- K822598 — TEFLON PIGTAIL/PERCUTANEOUS CARDIOVAS
- K822596 — VERTEX PERCUTANEOUS PUNCTURE NEEDLE
- K822597 — GUIDE WIRE
Data sourced from openFDA. This site is unofficial and independent of the FDA.