RESOUND PORTABLE PRESCRIPTIVE PROGRAMMING SYSTEM— 510(k) K931372

Substantially Equivalent

Resound Corp.

FDA 510(k) clearance K931372 for RESOUND PORTABLE PRESCRIPTIVE PROGRAMMING SYSTEM, Substantially Equivalent on 1993-11-03. Applicant: Resound Corp.. Device class: 1.

Clearance details

Applicant
Resound Corp.
Product code
Code ESD
Device class
Class 1
Regulation
21 CFR 874.3300
Advisory panel
Ear, Nose, Throat
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Redwood City, CA, US
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