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PM-8000 PATIENT MONITOR, MODEL 8000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032733
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2004
Days to Decision
181 days
Submission Type
Summary

PM-8000 PATIENT MONITOR, MODEL 8000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032733
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2004
Days to Decision
181 days
Submission Type
Summary