Snowden Pencer, Inc. is one of 25845 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Snowden Pencer, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SWITCHBLADE
1
Total
1
Cleared
0
Denied
Snowden Pencer, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tucker, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Snowden Pencer, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Snowden Pencer, Inc.
1 devices