Medical Device Manufacturer · US , Oregon , OH

R-Med, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1994

Total

Cleared

Denied

R-Med, Inc. has 9 FDA 510(k) cleared medical devices. Based in Oregon, US.

Historical record: 9 cleared submissions from 1994 to 2000. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - R-Med, Inc.

9 devices

1-9 of 9

Cleared Jul 17, 2000

RIZA BAND STRETCHER (RBS)-60000

K001236 · FHN

Gastroenterology & Urology · 90d

Cleared Jan 11, 1996

R-MED ABDOMINAL WALL ELEVATOR

K953360 · HET

Obstetrics & Gynecology · 178d

Cleared Nov 16, 1995

RIZA-RIBE NEEDLE (MODIFICATION)

Gastroenterology & Urology · 32d

Cleared May 11, 1995

R-MED MINI-RETRACTOR

K950108 · HET

Obstetrics & Gynecology · 120d

Cleared Mar 31, 1995

R-MED DISPOSABLE PLUG

K942411 · HET

Obstetrics & Gynecology · 315d

Cleared Dec 07, 1994

R-MED MOTORIZED LAPAROSCOPIC HANDLE

K945637 · GCJ

General & Plastic Surgery · 21d

Cleared Aug 29, 1994

MANUAL LAPAROSOPIC HANDLE, INTERCHANGEABLE LAPAROSCOPIC TOOL UNITS

K943818 · GEI

General & Plastic Surgery · 24d

Cleared Apr 25, 1994

RIZA-RIBE NEEDLE

K935031 · HET

Obstetrics & Gynecology · 187d

R-Med, Inc. - FDA 510(k) Cleared Devices

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