Ximed Medical Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ximed Medical Systems - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Ximed Medical Systems has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Santa Clara, US.
Historical record: 11 cleared submissions from 1989 to 1996.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ximed Medical Systems
11 devices
Cleared
Mar 11, 1996
BALLOON ELECTROSURGICAL PROBES AND DEVICES
General & Plastic Surgery
626d
Cleared
Mar 24, 1995
ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES
General & Plastic Surgery
95d
Cleared
Aug 26, 1994
HAND-HELD IRRIGATION PUMP
General & Plastic Surgery
408d
Cleared
May 05, 1994
SURGICAL TROCARS
General & Plastic Surgery
295d
Cleared
Aug 03, 1993
UNIVERSAL IRRIGATION & SUCTION TUBING SET
General Hospital
424d
Cleared
Sep 23, 1992
BIPOLAR ELECTROSURGICAL PROBES & INSTRUMENTS
General & Plastic Surgery
118d
Cleared
Sep 20, 1990
ELECTROPROBE SINGLE-USE SURGICAL PROBE
General & Plastic Surgery
31d
Cleared
Mar 22, 1990
LASER DELIVERY SYSTEMS, FIBEROPTICS & CONTACT TIPS
General & Plastic Surgery
50d
Cleared
Jun 22, 1989
INFRALASE-LASERGUIDE DELIVERY SYSTEM
General & Plastic Surgery
62d
Cleared
Apr 21, 1989
INFRALASE - LASERGUIDE DELIVERY SYSTEM
General & Plastic Surgery
65d
Cleared
Mar 17, 1989
MICROLASE CO2 LASER MICROMANIPULATOR
General & Plastic Surgery
14d