Last synced on 20 May 2022 at 11:05 pm

PULMONARY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781922
510(k) Type
Traditional
Applicant
VITALOGRAPH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1979
Days to Decision
92 days

PULMONARY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781922
510(k) Type
Traditional
Applicant
VITALOGRAPH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1979
Days to Decision
92 days