Site Microsurgical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Site Microsurgical Systems, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Site Microsurgical Systems, Inc. has 30 FDA 510(k) cleared ophthalmic devices. Based in Horsham, US.
Historical record: 30 cleared submissions from 1986 to 1994.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Site Microsurgical Systems, Inc.
30 devices
Cleared
Feb 16, 1994
MODIFIED SITE TXR SYSTEMS
Ophthalmic
457d
Cleared
Dec 06, 1993
MODIFIED SITE DISPOSABLE DIAPHRAGM CASSETTE
Ophthalmic
378d
Cleared
Nov 12, 1993
SITE'S CD II PHACOEMULSIFICATION HANDPIECE
Ophthalmic
212d
Cleared
Jun 03, 1992
IOLAB POWER I.V. POLE
Ophthalmic
85d
Cleared
May 08, 1992
180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.
Ophthalmic
88d
Cleared
Dec 17, 1991
PHACOEMULSIFICATION SYSTEM FOR OPHTHALMIC USE
Ophthalmic
168d
Cleared
Aug 28, 1991
SITE 90 TIP, I/A HANDPIECE .3MM SIDE OPEN/OPTH USE
Ophthalmic
68d
Cleared
May 22, 1991
SITE 20 GAUGE REUSABLE FIBER OPTIC CABLE
Ophthalmic
76d
Cleared
Feb 27, 1991
MODIFIED SITE PERISTALTIC FOOTSWITCH
Dental
75d
Cleared
Dec 05, 1990
SITE 19 GAUGE ULTRASONIC I/A PHACO NEEDLE
Ophthalmic
89d
Cleared
Dec 05, 1990
SITE PHACOEMULSIFICATION HANDPIECE
Ophthalmic
84d
Cleared
Nov 21, 1990
SITE DIAPHRAGM CASSETTE
Ophthalmic
70d