Medical Device Manufacturer · US , Mchenry , IL

Vertex Medical Corp. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1982

Total

Cleared

Denied

Vertex Medical Corp. has 21 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 21 cleared submissions from 1982 to 1984.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Vertex Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vertex Medical Corp.

21 devices

1-12 of 21

Cleared Apr 24, 1984

ESCHMANN DILATION CATHETER

K833742

General & Plastic Surgery · 181d

Cleared Feb 04, 1984

NEPHROSTOMY/BILIARY DRAINAGE BAG

K834476 · LJE

Gastroenterology & Urology · 46d

Cleared Nov 28, 1983

PROTECTIVE SLEEVE

K832380 · DYG

Cardiovascular · 132d

Cleared Jul 12, 1983

SIALOGRAPHY NEEDLE

K831666

General & Plastic Surgery · 50d

POLYETHYLENE MONITORING CONNECTORS

K830420 · DQO

Cardiovascular · 20d

Cleared Feb 18, 1983

TRANSLUCENT POLY. CATH. CONNECTOR AND

K830237 · DQO

Cardiovascular · 24d

Cleared Dec 30, 1982

BACKSTOP VALVE W/SIDE ARM

K823190 · DXT

Cardiovascular · 65d

Cleared Dec 30, 1982

DISPOSABLE PLASTIC STOPCOCK

K823191 · DXT

Cardiovascular · 65d

Cleared Dec 30, 1982

TUOHY-BORST ADAPTER W/SIDE ARM

K823192 · DXT

Cardiovascular · 65d

Cleared Dec 30, 1982

VERTEX MONITORING CATHETER

K823253 · DXT

Cardiovascular · 59d

Cleared Dec 30, 1982

REUSABLE METAL STOPCOCK

K823254 · DXT

Cardiovascular · 59d

Vertex Medical Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Vertex Medical Corp.

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