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EMBEDDING TOOL, MODEL TE-1000

Page Type
Cleared 510(K)
510(k) Number
K060897
510(k) Type
Traditional
Applicant
Medigroup, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2006
Days to Decision
106 days
Submission Type
Summary

EMBEDDING TOOL, MODEL TE-1000

Page Type
Cleared 510(K)
510(k) Number
K060897
510(k) Type
Traditional
Applicant
Medigroup, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2006
Days to Decision
106 days
Submission Type
Summary