Critical Patient Care, Inc. is one of 24646 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Critical Patient Care, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CRITICAL CARE ASSESSMENT
1
Total
1
Cleared
0
Denied
Critical Patient Care, Inc. has 1 FDA 510(k) cleared medical devices. Based in Endinburg, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Critical Patient Care, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Critical Patient Care, Inc.
1 devices