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GUMEASE DENTAL MOUTHPIECE

Page Type
Cleared 510(K)
510(k) Number
K072082
510(k) Type
Traditional
Applicant
Biomedevice , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
98 days
Submission Type
Summary

GUMEASE DENTAL MOUTHPIECE

Page Type
Cleared 510(K)
510(k) Number
K072082
510(k) Type
Traditional
Applicant
Biomedevice , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
98 days
Submission Type
Summary