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MEDIVISION I-VIEW PERSONAL VIDEO DISPLAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000669
510(k) Type
Traditional
Applicant
MEDIVISION ENDOSCOPY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2000
Days to Decision
88 days
Submission Type
Statement