Vitalograph , Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Vitalograph , Ltd. has 17 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Latest FDA clearance: Dec 2025. Active since 1979.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Vitalograph , Ltd.
17 devices
Cleared
Dec 03, 2025
VitaloJAK Clinic (Model 7100)
Anesthesiology
65d
Cleared
Oct 12, 1995
VITALOGRAPH 2110 SOFTWARE INTERFACE
Cardiovascular
227d
Cleared
Aug 12, 1993
ESCORT SPIROMETER
Anesthesiology
309d
Cleared
Jul 26, 1993
VITALOGRAPH DATA STORAGE SPIROMETER
Anesthesiology
200d
Cleared
Oct 15, 1991
VITALOGRAPH SPIROTRAC III
Anesthesiology
137d
Cleared
Aug 21, 1989
AEROSOL INHALATION MONITOR
Anesthesiology
98d
Cleared
May 05, 1989
VITALOGRAPH-BREATHCO MONITOR
Anesthesiology
24d
Cleared
Aug 29, 1988
VITALOGRAPH-ALPHA
Anesthesiology
362d
Cleared
Jun 02, 1988
VITALOGRAPH-EC60 HYDROGEN MONITOR
Chemistry
184d
Cleared
Jan 15, 1987
VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
Anesthesiology
133d
Cleared
May 06, 1986
DUAL-AID
Anesthesiology
55d
Cleared
Dec 24, 1985
VITALOGRAPH COMPACT
Anesthesiology
41d