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subpart-b—diagnostic-devices/

LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K214039
510(k) Type: Traditional
Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 3/22/2022
Days to Decision: 89 days
Submission Type: Summary

FDA Browser

subpart-b—diagnostic-devices/

LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K214039
510(k) Type: Traditional
Applicant: GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 3/22/2022
Days to Decision: 89 days
Submission Type: Summary