Medical Device Manufacturer · US , Clearwater , FL

Pace Tech, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1988
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: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Pace Tech, Inc. Filter by specialty or product code using the sidebar.

18 devices
1–12 of 18
VITALMAX 4000/MINIPACK 3100/3000
K951226 · DSK Computer, Blood-pressure · Cardiovascular
Nov 1996 612d
VITALMAX 4100
K953795 · CBS Analyzer, Gas, Halothane, Gaseous-phase (anesthetic Conc.) · Anesthesiology
Jul 1996 322d
HANDYPACK 911SC
K944541 · CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase · Anesthesiology
Feb 1995 160d
VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
K945385 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Jan 1995 89d
MINIPACK 911-STC
K925701 · CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase · Anesthesiology
Aug 1994 637d
MINIPACK 3100/3000 MODIFICATION
K934385 · DXN System, Measurement, Blood-pressure, Non-invasive · Cardiovascular
Aug 1994 335d
VITALMAX 4000
K933624 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Jul 1994 365d
VITALMAX 800-C
K930559 · CCK Analyzer, Gas, Carbon-dioxide, Gaseous-phase · Anesthesiology
Sep 1993 212d
MINI-PACK 911 SERIES
K912835 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Feb 1992 222d
VITALMAX 510/520
K912880 · DQA Oximeter · Anesthesiology
Nov 1991 136d
VITALMAX 830 SERIES
K913263 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Oct 1991 79d
VITALMAX 2100/2200
K905274 · DRT Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm) · Cardiovascular
Jul 1991 244d
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All18 Cardiovascular 9 Anesthesiology 9