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Finger Pulse Oximeter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163135
510(k) Type
Traditional
Applicant
SHENZHEN FITFAITH TECHNOLOGY CO.,LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/19/2017
Days to Decision
315 days
Submission Type
Summary

Finger Pulse Oximeter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163135
510(k) Type
Traditional
Applicant
SHENZHEN FITFAITH TECHNOLOGY CO.,LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/19/2017
Days to Decision
315 days
Submission Type
Summary