Laerdal Medical Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Laerdal Medical Corp. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1982 to 2000. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Laerdal Medical Corp. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Oct 06, 2000
RESUSCI INFLATE-A-SHIELD CPR BARRIER
Anesthesiology
120d
Cleared
Sep 05, 1996
TRACHLIGHT STYLET AND TRACHEAL LIGHTWAND
Anesthesiology
78d
Cleared
May 09, 1996
TRACHLIGHT STYLET & TRACHEAL LIGHTWAND (ORIGINAL APPLICATION NAME: STYLETT &...
Anesthesiology
205d
Cleared
Jan 04, 1996
HEARTSTART 911
Cardiovascular
92d
Cleared
May 09, 1995
LSU 2000 PORTABLE SUCTION UNIT
General & Plastic Surgery
88d
Cleared
Dec 02, 1993
LAERDAL(TM) POCKET MASK, MODIFICATION
Anesthesiology
205d
Cleared
May 03, 1990
HEARTSTART 3000
Cardiovascular
142d
Cleared
Mar 04, 1988
RESUSCI PATIENT FACE SHIELD
Anesthesiology
31d
Cleared
May 21, 1986
LAERDAL POCKET MASK
Anesthesiology
36d
Cleared
Mar 12, 1984
LAERDAL SUCTION UNIT
General & Plastic Surgery
62d
Cleared
Aug 20, 1982
MODULAIDE EMERG. CARDIAC LIFE SUPP. KT
Anesthesiology
14d