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GLOTTAL FREQUENCY ANALYSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841832
510(k) Type
Traditional
Applicant
TELTEC ELECTRONIC EQUIPMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1984
Days to Decision
76 days

GLOTTAL FREQUENCY ANALYSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841832
510(k) Type
Traditional
Applicant
TELTEC ELECTRONIC EQUIPMENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1984
Days to Decision
76 days