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Finger Pulse Oximeter

Page Type
Cleared 510(K)
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)
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