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THE MONITOR/DEMLAR MODEL MI-5000 AUDIOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913356
510(k) Type
Traditional
Applicant
MONITOR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1991
Days to Decision
128 days
Submission Type
Statement

THE MONITOR/DEMLAR MODEL MI-5000 AUDIOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913356
510(k) Type
Traditional
Applicant
MONITOR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1991
Days to Decision
128 days
Submission Type
Statement