Last synced on 23 September 2022 at 11:05 pm

MODEL 1309 AUDIO MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790664
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1979
Days to Decision
17 days

MODEL 1309 AUDIO MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790664
510(k) Type
Traditional
Applicant
LIFE-TECH INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1979
Days to Decision
17 days