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.

Uromed 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 - 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

FDA 510(k) Regulatory Record - Uromed Corp.

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