Medical Device Manufacturer · US , San Diego , CA

Pulse Metric, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1991

Total

Cleared

Denied

Pulse Metric, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 5 cleared submissions from 1991 to 2002. Primary specialty: Cardiovascular.

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

Pulse Metric, 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 - Pulse Metric, Inc.

5 devices

1-5 of 5