Primrose Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Primrose Medical, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1984 to 1989. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Primrose Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Primrose Medical, Inc.
14 devices
Cleared
Sep 29, 1989
URETHRAL AND URETERAL BALLOON DILATATORS
Gastroenterology & Urology
325d
Cleared
Sep 29, 1989
COLONIC BALLOON DIALATORS
Gastroenterology & Urology
325d
Cleared
Sep 29, 1989
BILIARY DIALATOR
Gastroenterology & Urology
325d
Cleared
Sep 29, 1989
ACHELASIA BALLOON DIALATOR
Gastroenterology & Urology
325d
Cleared
Sep 08, 1989
ENDOSCOPES & ACCESS.(SCLEROTHERAPY/TRANSBRONCHIAL)
Gastroenterology & Urology
304d
Cleared
Sep 08, 1989
ESOPHAGEAL AND PYLORIC BALLOON DIALATORS
Gastroenterology & Urology
304d
Cleared
Aug 26, 1988
LANCET, BLOOD
General & Plastic Surgery
11d
Cleared
Aug 04, 1988
CATHETER, INTRAVASCULAR
General Hospital
85d
Cleared
Jul 29, 1988
SET, INTRAVASCULAR
General Hospital
79d
Cleared
Jul 29, 1988
PRESSURE INFUSOR
General Hospital
79d
Cleared
Jul 13, 1988
ENTERAL FEEDING TUBES
Gastroenterology & Urology
63d
Cleared
Sep 24, 1987
NINJA SCALPEL
General & Plastic Surgery
24d