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AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942358
510(k) Type
Traditional
Applicant
M.P. VIDEO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1994
Days to Decision
83 days
Submission Type
Statement