Beacon Laboratories, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Beacon Laboratories, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Westminster, US.
Historical record: 18 cleared submissions from 1989 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) cleared devices by Beacon Laboratories, Inc.
18 devices
Cleared
Mar 11, 1994
FLEXIBLE EXTENDER
General & Plastic Surgery
416d
Cleared
Jun 25, 1993
ARGON HANDPIECES
General & Plastic Surgery
144d
Cleared
Apr 20, 1993
DISPOSABLE ELECTROSURGERY BALL ELECTRODE
General & Plastic Surgery
159d
Cleared
Jan 15, 1993
SESQUIPOLAR(TM) MIS ELECTRODE
General & Plastic Surgery
245d
Cleared
Dec 24, 1992
DISPOSABLE HAND-SWITCHING ESU PENCIL
General & Plastic Surgery
48d
Cleared
Mar 13, 1992
MIS ELECTROSURGICAL ELECTRODES
General & Plastic Surgery
80d
Cleared
Feb 03, 1992
GSU HANDPIECE ADAPTER
General & Plastic Surgery
25d
Cleared
Nov 19, 1991
PRESSURE GUARD
General & Plastic Surgery
88d
Cleared
Jul 22, 1991
ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
General & Plastic Surgery
210d
Cleared
Dec 13, 1990
ACTIVE ADAPTER
General & Plastic Surgery
72d
Cleared
Nov 21, 1990
ARGON BEAM LAPAROSCOPIC ELECTRODE
General & Plastic Surgery
135d
Cleared
Sep 28, 1990
BEAMER 1,2,4,6, AND 8
General & Plastic Surgery
43d