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MODULE PERSONAL EAR (COMPRESSION)

Page Type
Cleared 510(K)
510(k) Number
K790094
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1979
Days to Decision
10 days

MODULE PERSONAL EAR (COMPRESSION)

Page Type
Cleared 510(K)
510(k) Number
K790094
510(k) Type
Traditional
Applicant
QUALITONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1979
Days to Decision
10 days