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NU-VOIS BATTERY POWERED ARTIFICIAL LARYNX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934483
510(k) Type
Traditional
Applicant
MOUNTAIN PRECISION MFG. LTD. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
183 days
Submission Type
Summary

NU-VOIS BATTERY POWERED ARTIFICIAL LARYNX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934483
510(k) Type
Traditional
Applicant
MOUNTAIN PRECISION MFG. LTD. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
183 days
Submission Type
Summary