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EsoCheck Cell Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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