OTICON /PRIMOFOCUS (PF)— 510(k) K960284

Substantially Equivalent

Oticon, Inc.

FDA 510(k) clearance K960284 for OTICON /PRIMOFOCUS (PF), Substantially Equivalent on 1996-03-07. Applicant: Oticon, Inc..

Clearance details

Applicant: Oticon, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1996-01-19
Decision date: 1996-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Somerset, NJ, US

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