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Fingertip Pulse Oximeter MD300CN310

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161560
510(k) Type
Traditional
Applicant
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/5/2016
Days to Decision
121 days
Submission Type
Summary

Fingertip Pulse Oximeter MD300CN310

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K161560
510(k) Type
Traditional
Applicant
BEIJING CHOICE ELECTRONIC TECHNOLOGY CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/5/2016
Days to Decision
121 days
Submission Type
Summary