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AED RESECTOSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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