Marina Medical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Marina Medical Instruments, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Marina Medical Instruments, Inc. has 5 FDA 510(k) cleared medical devices. Based in Hollywood, US.
Historical record: 5 cleared submissions from 2001 to 2005. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Marina Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Marina Medical Instruments, Inc.
5 devices
Cleared
May 10, 2005
MARINA MEDICAL FINGER PROTECTORS
General Hospital
235d
Cleared
Nov 18, 2003
MARINA MEDICAL SILICONE PESSARY
Obstetrics & Gynecology
194d
Cleared
Apr 08, 2003
MAS WITH OR WITHOUT SYRINGE
Obstetrics & Gynecology
305d
Cleared
Feb 03, 2003
HEMORRHAGE OCCLUDER PIN (HOP), MODEL 337-247
General & Plastic Surgery
89d
Cleared
Apr 11, 2001
UTERINE MANIPULATOR INJECTOR CANNULA, MODEL R57-450
Obstetrics & Gynecology
70d