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BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230

Page Type
Cleared 510(K)
510(k) Number
K062603
510(k) Type
Traditional
Applicant
BIOSPACE CORPORATION LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2007
Days to Decision
167 days
Submission Type
Summary

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230

Page Type
Cleared 510(K)
510(k) Number
K062603
510(k) Type
Traditional
Applicant
BIOSPACE CORPORATION LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2007
Days to Decision
167 days
Submission Type
Summary