Epocal, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Epocal, Inc. - FDA 510(k) Cleared Devices
Recent clearances: epoc Blood Analysis System, epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
7
Total
7
Cleared
0
Denied
Epocal, Inc. has 7 FDA 510(k) cleared medical devices. Based in Ottawa, CA.
Historical record: 7 cleared submissions from 2006 to 2020. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Epocal, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Epocal, Inc.
7 devices
Cleared
Jun 05, 2020
epoc Blood Analysis System
Chemistry
140d
Cleared
Jan 17, 2018
epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
Chemistry
264d
Cleared
Oct 05, 2012
EPOC CHLORIDE TEST AND EPOC CREATININE TEST
Chemistry
291d
Cleared
Jun 09, 2010
EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBE
Chemistry
231d
Cleared
Mar 30, 2010
BLOOD COLLECTION TUBE SAMPLES FOR USE WITH POINT OF CARE BLOOD ANALYZER
Chemistry
195d
Cleared
Jun 24, 2009
BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD
Chemistry
160d
Cleared
Sep 27, 2006
EPOC BLOOD ANALYSIS SYSTEM
Chemistry
111d