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EsoCheck Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K210137
510(k) Type
Special
Applicant
Lucid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/18/2021
Days to Decision
30 days
Submission Type
Summary

EsoCheck Cell Collection Device

Page Type
Cleared 510(K)
510(k) Number
K210137
510(k) Type
Special
Applicant
Lucid Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/18/2021
Days to Decision
30 days
Submission Type
Summary