Chestnut Medical Technologies, Inc. is one of 22273 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chestnut Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX, MARKSMANN CATHETER, ALLIGATOR RETRIEVAL DEVICE (ARD)
3
Total
3
Cleared
0
Denied
Chestnut Medical Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 3 cleared submissions from 2005 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Chestnut Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kema Quality B.V. as regulatory consultant.
FDA 510(k) Regulatory Record - Chestnut Medical Technologies, Inc.
3 devices