Pulse Biomedical, Inc. is one of 20565 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulse Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: QRS CARD S-T SEGMENT ANALYSIS PATIENT MONITORING SYSTEM MODEL: QRS CARD USB, QRS-CARD CARDIOLOGY SUITE, PULSE BIOMEDICAL INC, QRS CARD S-T SEGMENT ANALYSIS MONITORING SYSTEM
3
Total
3
Cleared
0
Denied
Pulse Biomedical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Norristown, US.
Historical record: 3 cleared submissions from 1998 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pulse Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Pulse Biomedical, Inc.
3 devices