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PERSONAL AMPLIFIER MODULE

Page Type
Cleared 510(K)
510(k) Number
K830790
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
120 days

PERSONAL AMPLIFIER MODULE

Page Type
Cleared 510(K)
510(k) Number
K830790
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
120 days