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EsoCheck Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K230339
510(k) Type
Special
Applicant
Lucid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/24/2023
Days to Decision
17 days
Submission Type
Summary

EsoCheck Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K230339
510(k) Type
Special
Applicant
Lucid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/24/2023
Days to Decision
17 days
Submission Type
Summary