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M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100046
510(k) Type
Traditional
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/8/2010
Days to Decision
90 days
Submission Type
Summary

M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100046
510(k) Type
Traditional
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/8/2010
Days to Decision
90 days
Submission Type
Summary