Pace Tech, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Pace Tech, Inc. has 18 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Historical record: 18 cleared submissions from 1988 to 1996. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Pace Tech, Inc. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Nov 21, 1996
VITALMAX 4000/MINIPACK 3100/3000
Cardiovascular
612d
Cleared
Jul 01, 1996
VITALMAX 4100
Anesthesiology
322d
Cleared
Feb 22, 1995
HANDYPACK 911SC
Anesthesiology
160d
Cleared
Jan 31, 1995
VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
Cardiovascular
89d
Cleared
Aug 11, 1994
MINIPACK 911-STC
Anesthesiology
637d
Cleared
Aug 10, 1994
MINIPACK 3100/3000 MODIFICATION
Cardiovascular
335d
Cleared
Jul 19, 1994
VITALMAX 4000
Cardiovascular
365d
Cleared
Sep 03, 1993
VITALMAX 800-C
Anesthesiology
212d
Cleared
Feb 03, 1992
MINI-PACK 911 SERIES
Cardiovascular
222d
Cleared
Nov 14, 1991
VITALMAX 510/520
Anesthesiology
136d
Cleared
Oct 10, 1991
VITALMAX 830 SERIES
Cardiovascular
79d
Cleared
Jul 17, 1991
VITALMAX 2100/2200
Cardiovascular
244d
Cleared
Aug 28, 1990
VITALMAX 500 PULSE OXIMETER W/TEMP. AND RESPIRA.
Anesthesiology
174d
Cleared
Jul 18, 1990
VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE
Cardiovascular
169d
Cleared
Apr 30, 1990
VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE
Anesthesiology
24d
Cleared
Apr 04, 1990
OXIMAX 700
Anesthesiology
40d
Cleared
Mar 28, 1990
OXIMAX 100
Anesthesiology
34d
Cleared
Mar 22, 1988
VITAL SYSTEM
Cardiovascular
56d