Alm Surgical Equipment, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Alm Surgical Equipment, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Pasadena, US.
Historical record: 10 cleared submissions from 1988 to 1998.
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 Alm Surgical Equipment, Inc.
10 devices
Cleared
Sep 22, 1998
ALM PRISMALIX (PRX) SURGICAL LIGHT
General & Plastic Surgery
102d
Cleared
Jul 30, 1996
DRAGER GEMINA WALL-MOUNTED WORKPLACE
General & Plastic Surgery
76d
Cleared
Jul 26, 1996
DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEM
General & Plastic Surgery
81d
Cleared
Nov 04, 1994
MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE
Gastroenterology & Urology
17d
Cleared
Jul 13, 1994
DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032E
General & Plastic Surgery
76d
Cleared
Jan 12, 1993
ALM ILLUMINATOR SERIES LIGHT SYSTEM
General & Plastic Surgery
236d
Cleared
Nov 27, 1992
DRAGER DVE 4000 SERIES SYSTEM
General & Plastic Surgery
255d
Cleared
Oct 01, 1992
BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHT
General & Plastic Surgery
167d
Cleared
Oct 13, 1988
ALM OPERATING TABLES
General & Plastic Surgery
21d
Cleared
Jul 18, 1988
ALM SURGICAL LAMPS
General & Plastic Surgery
24d