Epimed International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epimed International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Percutaneous Introducer, Rulo Radiofrequency Lesion Probe
14
Total
14
Cleared
0
Denied
Epimed International, Inc. has 14 FDA 510(k) cleared anesthesiology devices. Based in Johnstown, US.
Historical record: 14 cleared submissions from 1998 to 2020.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Epimed International, Inc.
14 devices
Cleared
Apr 27, 2020
Percutaneous Introducer
Anesthesiology
48d
Cleared
Mar 08, 2019
Rulo Radiofrequency Lesion Probe
Neurology
29d
Cleared
May 28, 2014
SPIROL BLOCK (19 GA. OPEN END MODELS), (20 GA. OPEN END MODELS), (19 GA....
Anesthesiology
212d
Cleared
Feb 17, 2006
RX EPIDURAL NEEDLE
Anesthesiology
79d
Cleared
Aug 26, 2005
STINGRAY EPIDURAL CATHETER CONNECTOR
Anesthesiology
112d
Cleared
Aug 22, 2005
FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837
Anesthesiology
45d
Cleared
Mar 31, 2005
FLEXIBLE SPINAL NEEDLE
Anesthesiology
106d
Cleared
Sep 16, 2004
RF INTRODUCTION CANNULA
Neurology
149d
Cleared
Aug 24, 2004
PENCIL POINT NEEDLE
Anesthesiology
47d
Cleared
Aug 15, 2003
VERSA-KATH EPIDURAL CATHETER, MODEL 156-2124
Anesthesiology
329d
Cleared
Apr 03, 2003
TUOHY EPIDURAL NEEDLE
Anesthesiology
41d
Cleared
Jul 30, 2002
QUINCKE SPINAL NEEDLE
Anesthesiology
39d