Epocal, Inc.
Epocal, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2020, with 1 FDA device recall on record.
Top product codes for Epocal, Inc.
FDA recalls by Epocal, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Epocal, Inc.
- K200107 — epoc Blood Analysis System
- K171247 — epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
- K113726 — EPOC CHLORIDE TEST AND EPOC CREATININE TEST
- K093297 — EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBE
- K092849 — BLOOD COLLECTION TUBE SAMPLES FOR USE WITH POINT OF CARE BLOOD ANALYZER
- K090109 — BLOOD GAS, ELECTROLYTE AND METABOLITE TEST CARD
- K061597 — EPOC BLOOD ANALYSIS SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.