FDA 510(k) Applications Submitted by OTICON, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K960284 01/19/1996 OTICON /PRIMOFOCUS (PF) OTICON, INC.
K961059 03/18/1996 DIGIFOCUS COMPACT OTICON, INC.
K973886 10/14/1997 OTICON DIGISOUND COMPACT OTICON, INC.
K964683 11/22/1996 DIGIFOCUS ITE OTICON, INC.
K973885 10/14/1997 OTICON DIGISOUND ITE OTICON, INC.


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