Lucid Diagnostics, Inc.
Lucid Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2023, with 2 FDA device recalls on record.
Top product codes for Lucid Diagnostics, Inc.
FDA recalls by Lucid Diagnostics, Inc.
- Z-1900-2024 — Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A
- Z-1899-2024 — Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter, 20 pores/inch) Model/Catalog Number: EC20T20VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: No
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 Lucid Diagnostics, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.