Medical Device Manufacturer · US , Norwood , MA

Uromed Corp. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1997

Total

Cleared

Denied

Uromed Corp. has 10 FDA 510(k) cleared medical devices. Based in Norwood, US.

Historical record: 10 cleared submissions from 1997 to 2001. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Uromed Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Uromed Corp.

10 devices

1-10 of 10

Cleared Apr 20, 2001

MODIFICATION TO CAVERMAP SURGICAL AID

K010213 · ETN

Ear, Nose, Throat · 87d

Cleared Feb 01, 2001

MODIFICATION TO CAVERMAP SURGICAL AID

K010098 · FGM

Gastroenterology & Urology · 21d

Cleared Apr 21, 2000

CAVERMAP SURGICAL AID

K000507 · ETN

Ear, Nose, Throat · 66d

Cleared Feb 11, 2000

CAVERMAP SURGICAL AID

K993436 · FGM

Gastroenterology & Urology · 122d

Cleared May 13, 1999

UROMED BRACHYTHERAPHY IODINE-125 SOURCES

Obstetrics & Gynecology · 87d

Cleared Mar 31, 1998

UROMED PATCH

K974600 · MNG

Gastroenterology & Urology · 112d

Cleared Jan 30, 1998

UROMED NEEDLE GRASPER

K974137 · OCW

Gastroenterology & Urology · 88d

Cleared Oct 27, 1997

URO MED NERVE STIMULATOR

K970971 · ETN

Ear, Nose, Throat · 224d

Cleared Aug 01, 1997

UROMED ALTERNATIVE BLADDER CONTROL CONTINENCE DEVICE(ABCPN-0026)

K971992 · FHA

Gastroenterology & Urology · 64d

Uromed Corp. - FDA 510(k) Cleared Devices

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