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PM SERIES PATIENT MONITORS, MODELS PM-9000 EXPRESS AND PM-8000 EXPRESS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070791
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2007
Days to Decision
96 days
Submission Type
Summary

PM SERIES PATIENT MONITORS, MODELS PM-9000 EXPRESS AND PM-8000 EXPRESS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070791
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2007
Days to Decision
96 days
Submission Type
Summary