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PERSONAL AMPLIFIER MODEL ULTRA HELIX

Page Type
Cleared 510(K)
510(k) Number
K893433
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1989
Days to Decision
43 days

PERSONAL AMPLIFIER MODEL ULTRA HELIX

Page Type
Cleared 510(K)
510(k) Number
K893433
510(k) Type
Traditional
Applicant
ELECTONE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1989
Days to Decision
43 days