Medical Device Manufacturer · US , Indianapolis , IN

Catheter Research, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1994

8

Total

8

Cleared

0

Denied

Catheter Research, Inc. has 8 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 8 cleared submissions from 1994 to 2013. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Catheter Research, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Catheter Research, Inc.

8 devices

1-8 of 8

Cleared Jan 31, 2013

THE ADVANCE CATHETER FOR HSG AND SIS

Obstetrics & Gynecology · 105d

Cleared Mar 21, 2012

INTRAUTERINE INSEMINATION (IUI) CATHETER

Obstetrics & Gynecology · 63d

Cleared Dec 11, 2003

H/S CATHETER SET

Obstetrics & Gynecology · 91d

Cleared Apr 17, 2002

UTERINE INJECTOR

Obstetrics & Gynecology · 79d

Cleared Mar 19, 1998

DISPOSABLE ESOPHAGEAL STETHOSCOPE

Anesthesiology · 162d

Cleared Feb 02, 1998

UTERINE MANIPULATOR/INJECTOR

Obstetrics & Gynecology · 75d

Cleared Apr 14, 1995

DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLING

Anesthesiology · 22d

Cleared Dec 27, 1994

DISPOSABLE GAS SAMPLING LINES

Anesthesiology · 15d