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PERSONAL AMPLIFIER MODEL ULTRA HELIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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