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A SLEEP ASSESSMENT DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792305
510(k) Type
Traditional
Applicant
FARRALL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1979
Days to Decision
34 days

A SLEEP ASSESSMENT DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792305
510(k) Type
Traditional
Applicant
FARRALL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1979
Days to Decision
34 days