Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact