Medical Device Manufacturer · US , Santa Ana , CA

Accucore, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1987

Total

Cleared

Denied

Accucore, Inc. has 9 FDA 510(k) cleared medical devices. Based in Santa Ana, US.

Historical record: 9 cleared submissions from 1987 to 1995. Primary specialty: Cardiovascular.

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

Accucore, 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 - Accucore, Inc.

9 devices

1-9 of 9

Cleared Jan 30, 1995

PACIFIC COMMUNICATIONS MODEL 1100

K942147 · DSI

Cardiovascular · 272d

Cleared Feb 25, 1993

MODEL 2041-PC/ST CARDIAC TELEMETRY MONITOR

K925411 · DSI

Cardiovascular · 122d

Cleared Jan 28, 1992

DATASCOPE MODEL VISA CENTRAL MONITOR

K913576 · DSI

Cardiovascular · 169d

PCI MODEL 2041-B TELEMETRY MONITOR

K896775 · DSI

Cardiovascular · 167d

Cleared May 17, 1990

PCI MODEL 2041-PC TELEMETRY MONITOR

K901031 · DRT

Cardiovascular · 72d

Cleared Apr 04, 1990

PCI MODEL 2041-PC TELEMETRY MONITOR W/ARRHYTHMIA

K901032 · DPS

Cardiovascular · 29d

Cleared Oct 02, 1989

PCI MODEL 2041-A TELEMETRY MONITOR

K894340 · DXH

Cardiovascular · 80d

Cleared Dec 18, 1987

PCI MODEL RS100 TELEMETRY MONITOR

K874387 · DXH

Cardiovascular · 53d

Accucore, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Accucore, Inc.

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