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EdgeLife Handheld Wireless Ultrasound System (E8200); EdgeLife Handheld Wireless Ultrasound System (E8220)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234153
510(k) Type
Traditional
Applicant
EdgeLife Technologies LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2024
Days to Decision
264 days
Submission Type
Summary

EdgeLife Handheld Wireless Ultrasound System (E8200); EdgeLife Handheld Wireless Ultrasound System (E8220)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234153
510(k) Type
Traditional
Applicant
EdgeLife Technologies LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2024
Days to Decision
264 days
Submission Type
Summary