Medical Device Manufacturer · US , West Warwick , RI

Astro-Med, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1989

Total

Cleared

Denied

Astro-Med, Inc. has 13 FDA 510(k) cleared medical devices. Based in West Warwick, US.

Historical record: 13 cleared submissions from 1989 to 2008. Primary specialty: Cardiovascular.

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

Astro-Med, 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 - Astro-Med, Inc.

13 devices

1-12 of 13

GRASS BRAINWAVE SOFTWARE

K970951 · OLV

Neurology · 66d

Cleared Dec 12, 1996

GRASS MODEL 15 NEURODATA AMPLIFIER SYSTEM

Cardiovascular · 398d

ASC-954 INTEGRATOR AMPLIFIER

K896164 · GWK

Neurology · 90d

Cleared Jan 18, 1990

ASTRO-MED ASC-951 PRESSURE PROCESSOR

K894295 · DRQ

Cardiovascular · 209d

Cleared Dec 13, 1989

MT96000 PAPER CHART RECORDER

K894736 · DSF

Cardiovascular · 139d

Cleared Sep 18, 1989

ASC-952 PHYSIOLOGICAL AMPLIFIER

K894735 · DRR

Cardiovascular · 53d

Cleared Aug 03, 1989

ASC-950 ECG AMPLIFIER

K894161 · DRR

Cardiovascular · 50d

Astro-Med, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Astro-Med, Inc.

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