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AMENDMENTS TO MULTIFOCUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951002
510(k) Type
Traditional
Applicant
OTICON A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
9/18/1995
Days to Decision
203 days
Submission Type
Statement