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MODIFICATION TO PM-8000 PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043348
510(k) Type
Special
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2005
Days to Decision
31 days
Submission Type
Summary

MODIFICATION TO PM-8000 PATIENT MONITOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043348
510(k) Type
Special
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2005
Days to Decision
31 days
Submission Type
Summary