Last synced on 14 November 2025 at 11:06 pm

RESOUND REAL EAR LOUDNESS MAPPING (RELM) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960229
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
50 days
Submission Type
Summary

RESOUND REAL EAR LOUDNESS MAPPING (RELM) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K960229
510(k) Type
Traditional
Applicant
RESOUND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
50 days
Submission Type
Summary