Medical Device Manufacturer · US , Clearwater , FL

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

18 submissions · 18 cleared · Since 1988

Total

Cleared

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.

Pace Tech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pace Tech, Inc.

18 devices

1-12 of 18

Cleared Nov 21, 1996

VITALMAX 4000/MINIPACK 3100/3000

K951226 · DSK

Cardiovascular · 612d

Cleared Jul 01, 1996

VITALMAX 4100

K953795 · CBS

Anesthesiology · 322d

Cleared Feb 22, 1995

HANDYPACK 911SC

K944541 · CCK

Anesthesiology · 160d

Cleared Jan 31, 1995

VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300

Anesthesiology · 637d

Cleared Aug 10, 1994

MINIPACK 3100/3000 MODIFICATION

K934385 · DXN

Cardiovascular · 335d

Cleared Jul 19, 1994

VITALMAX 4000

K933624 · MHX

Cardiovascular · 365d

Cleared Sep 03, 1993

VITALMAX 800-C

K930559 · CCK

Anesthesiology · 212d

Cleared Feb 03, 1992

MINI-PACK 911 SERIES

K912835 · MHX

Cardiovascular · 222d

Cleared Nov 14, 1991

VITALMAX 510/520

K912880 · DQA

Anesthesiology · 136d

Cardiovascular · 244d

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

FDA 510(k) Regulatory Record - Pace Tech, Inc.

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