Pace Tech, Inc.
Pace Tech, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1996.
Top product codes for Pace Tech, Inc.
Recent clearances by Pace Tech, Inc.
- K951226 — VITALMAX 4000/MINIPACK 3100/3000
- K953795 — VITALMAX 4100
- K944541 — HANDYPACK 911SC
- K945385 — VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300
- K925701 — MINIPACK 911-STC
- K934385 — MINIPACK 3100/3000 MODIFICATION
- K933624 — VITALMAX 4000
- K930559 — VITALMAX 800-C
- K912835 — MINI-PACK 911 SERIES
- K912880 — VITALMAX 510/520
- K913263 — VITALMAX 830 SERIES
- K905274 — VITALMAX 2100/2200
- K901066 — VITALMAX 500 PULSE OXIMETER W/TEMP. AND RESPIRA.
- K900451 — VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE
- K901612 — VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE
- K900866 — OXIMAX 700
- K900843 — OXIMAX 100
- K880351 — VITAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.