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FUJIFILM Ultrasonic Processor SP-900 and FUJIFILM Ultrasonic Probe PB2020-M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171207
510(k) Type
Traditional
Applicant
FUJIFILM Medical Systems U.S.A., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2018
Days to Decision
261 days
Submission Type
Summary

FUJIFILM Ultrasonic Processor SP-900 and FUJIFILM Ultrasonic Probe PB2020-M

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171207
510(k) Type
Traditional
Applicant
FUJIFILM Medical Systems U.S.A., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2018
Days to Decision
261 days
Submission Type
Summary