Synemed, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Synemed, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1981 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Synemed, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Nov 17, 1995
FIELD TREND
Ophthalmic
81d
Cleared
Oct 15, 1985
THE FIELDMASTER MODEL 275
Ophthalmic
97d
Cleared
Dec 03, 1983
DERMATOLOGY HANDPIECE-OPHTH LASER
Ophthalmic
73d
Cleared
Jun 08, 1983
SYNEVAC VACUUM SOURCE UNIT
General & Plastic Surgery
65d
Cleared
Jan 03, 1983
OPTHALAS PHOTOCOAGULATOR
Radiology
41d
Cleared
Oct 18, 1982
MODEL 200 SQUID
Ophthalmic
21d
Cleared
Dec 14, 1981
SYNEVAC VACUUM CURETTAGE SYSTEMS
Obstetrics & Gynecology
27d
Cleared
Sep 08, 1981
SCOPE MASTER
Obstetrics & Gynecology
125d