Medical Device Manufacturer · US , Mt. Vernon , NY

Multigon Industries, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1985

8

Total

8

Cleared

0

Denied

Multigon Industries, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mt. Vernon, US.

Historical record: 8 cleared submissions from 1985 to 2005.

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

FDA 510(k) Regulatory Record - Multigon Industries, Inc.

8 devices

1-8 of 8

Cleared Aug 29, 2005

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H

Radiology · 28d

Cleared Jul 28, 2005

POCKET TRANSCRANIAL AND VASCULAR DOPPLER SPECTRUM ANALYZER, MODEL 500P

Radiology · 30d

Cleared Jun 24, 1991

MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR

Obstetrics & Gynecology · 47d

Cleared Jan 05, 1990

MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER

Obstetrics & Gynecology · 652d

Cleared Nov 29, 1988

MODEL 500V VASCULAR SPECTRUM ANALYZER

Radiology · 147d

Cleared Jun 24, 1987

MODEL 600 VASCULAR DUPLEX IMAGER

Cardiovascular · 282d

Cleared May 05, 1986

MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER

Cardiovascular · 90d

Cleared Dec 23, 1985

TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG

Obstetrics & Gynecology · 181d