Deschutes Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Deschutes Medical Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Deschutes Medical Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Bend, US.
Historical record: 8 cleared submissions from 1995 to 2000. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Deschutes Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Deschutes Medical Products, Inc.
8 devices
Cleared
Sep 18, 2000
PELVX GELLHORN VAGINAL PESSARY 603-608
Obstetrics & Gynecology
48d
Cleared
Mar 01, 2000
REFLEX TREATMENT SYSTEM
Gastroenterology & Urology
90d
Cleared
May 24, 1999
PELVX INCONTINENCE DISH, MODEL 301-306
Obstetrics & Gynecology
89d
Cleared
Apr 27, 1998
PELVX RING, PELVX RING WITH SUPPORT
Obstetrics & Gynecology
178d
Cleared
Apr 27, 1998
PELVX INCONTINENCE RING
Obstetrics & Gynecology
178d
Cleared
Apr 27, 1998
PELVX DONUT, PELVX CUBE
Obstetrics & Gynecology
178d
Cleared
Aug 09, 1995
PERIPUMP
Gastroenterology & Urology
687d
Cleared
Jun 06, 1995
SURGACTIVATOR
Gastroenterology & Urology
63d