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RESNICK EMITTER, ARTIFICIAL LARYNX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854158
510(k) Type
Traditional
Applicant
DYNAMED AUDIO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1985
Days to Decision
63 days

RESNICK EMITTER, ARTIFICIAL LARYNX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854158
510(k) Type
Traditional
Applicant
DYNAMED AUDIO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1985
Days to Decision
63 days