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Pace Tech, Inc.

18 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
VITALMAX 4000/MINIPACK 3100/3000 (K951226)Pace Tech, Inc.1996-11-21
VITALMAX 4100 (K953795)Pace Tech, Inc.1996-07-01
HANDYPACK 911SC (K944541)Pace Tech, Inc.1995-02-22
VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300 (K945385)Pace Tech, Inc.1995-01-31
MINIPACK 911-STC (K925701)Pace Tech, Inc.1994-08-11
MINIPACK 3100/3000 MODIFICATION (K934385)Pace Tech, Inc.1994-08-10
VITALMAX 4000 (K933624)Pace Tech, Inc.1994-07-19
VITALMAX 800-C (K930559)Pace Tech, Inc.1993-09-03
MINI-PACK 911 SERIES (K912835)Pace Tech, Inc.1992-02-03
VITALMAX 510/520 (K912880)Pace Tech, Inc.1991-11-14
VITALMAX 830 SERIES (K913263)Pace Tech, Inc.1991-10-10
VITALMAX 2100/2200 (K905274)Pace Tech, Inc.1991-07-17
VITALMAX 500 PULSE OXIMETER W/TEMP. AND RESPIRA. (K901066)Pace Tech, Inc.1990-08-28
VITALMAX 800 NON-INVASIVE VITAL SIGN MONITOR/PULSE (K900451)Pace Tech, Inc.1990-07-18
VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE (K901612)Pace Tech, Inc.1990-04-30
OXIMAX 700 (K900866)Pace Tech, Inc.1990-04-04
OXIMAX 100 (K900843)Pace Tech, Inc.1990-03-28
VITAL SYSTEM (K880351)Pace Tech, Inc.1988-03-22

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Every clearance here is in the API, with alerts when new ones post.