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AED RESECTOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K102663
510(k) Type
Traditional
Applicant
National Advanced Endoscopy Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2010
Days to Decision
106 days
Submission Type
Summary

AED RESECTOSCOPE

Page Type
Cleared 510(K)
510(k) Number
K102663
510(k) Type
Traditional
Applicant
National Advanced Endoscopy Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2010
Days to Decision
106 days
Submission Type
Summary