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BIONET BM3PLUS PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K082008
510(k) Type
Traditional
Applicant
BIONET CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2008
Days to Decision
149 days
Submission Type
Summary

BIONET BM3PLUS PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K082008
510(k) Type
Traditional
Applicant
BIONET CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2008
Days to Decision
149 days
Submission Type
Summary