Olsen Electrosurgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Olsen Electrosurgical, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Olsen Electrosurgical, Inc. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Concord, US.
Historical record: 11 cleared submissions from 1988 to 1994.
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 - Olsen Electrosurgical, Inc.
11 devices
Cleared
Apr 21, 1994
INSULATED SPECULUM W/ SMOKE EVACUATOR OPTION
Obstetrics & Gynecology
714d
Cleared
Apr 15, 1992
OLSEN LAPAROSCOPIC INSTR, DISPOSABLE, SINGLE USE
General & Plastic Surgery
308d
Cleared
Dec 23, 1991
TEFLON COATED ELECTRODES/ELECTRODES HANDLES
General & Plastic Surgery
164d
Cleared
Nov 01, 1991
SMOKE/ODOR EVACUATOR #757
General Hospital
142d
Cleared
Jan 13, 1989
#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHES
General & Plastic Surgery
28d
Cleared
Jan 13, 1989
600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE
General & Plastic Surgery
28d
Cleared
Oct 24, 1988
#875 DISPOSABLE BIOPOLAR CABLE
General & Plastic Surgery
24d
Cleared
Oct 24, 1988
MODIFIED OLSEN #770 DISPOSABLE HOLSTER
General & Plastic Surgery
24d
Cleared
Oct 24, 1988
#920 DISPOSABLE TUR CABLE
General & Plastic Surgery
24d
Cleared
Oct 24, 1988
MODIFIED OLSEN 755/756 SWITCHPENS
General & Plastic Surgery
24d
Cleared
Oct 24, 1988
#820/821 BIPOLAR FORCEPS
General & Plastic Surgery
24d