Non-Invasive Monitoring Systems, Inc. - FDA 510(k) Cleared Devices

Non-Invasive Monitoring Systems, Inc. specializes in non-invasive monitoring and respiratory measurement devices. The company operated with a manufacturing facility in Washington, US.

The company received 6 FDA 510(k) clearances from 6 total submissions, with no denied submissions on record. Clearances span from 1989 to 2001, covering cardiovascular and anesthesiology device categories. The company's regulatory activity is historical; no clearances have been issued in more than two decades.

Notable cleared devices include respiratory monitoring and event processing software platforms, as well as waveform capture and central monitoring systems. These products supported clinical applications in cardiac monitoring and anesthesia management.

For detailed information on specific device names, product codes, and individual clearance dates, please review the complete 510(k) clearance record.