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RONDOFLEX PLUS 360

Page Type
Cleared 510(K)
510(k) Number
K042872
510(k) Type
Special
Applicant
Kavo America Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2004
Days to Decision
36 days
Submission Type
Summary

RONDOFLEX PLUS 360

Page Type
Cleared 510(K)
510(k) Number
K042872
510(k) Type
Special
Applicant
Kavo America Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2004
Days to Decision
36 days
Submission Type
Summary