Vitalograph, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Vitalograph, Inc. has 5 FDA 510(k) cleared medical devices. Based in Lenexa, US.
Historical record: 5 cleared submissions from 1994 to 2000. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vitalograph, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Sep 08, 2000
VITALOGRAPH BASE STATION
Anesthesiology
199d
Cleared
Feb 04, 2000
VITALOGRAPH MICRO
Anesthesiology
287d
Cleared
Dec 14, 1995
ELECTRONIC FLOW METER
Anesthesiology
506d
Cleared
Aug 04, 1995
VITALOGRAPH MODEL 2120
Anesthesiology
242d
Cleared
Jul 13, 1994
DISPOSABLE BACTERIOLOGICAL FILTER
Anesthesiology
30d