Last synced on 29 August 2025 at 11:05 pm

CHEST FLUID MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772092
510(k) Type
Traditional
Applicant
DYNATECH RESEARCH & DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1977
Days to Decision
11 days

CHEST FLUID MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772092
510(k) Type
Traditional
Applicant
DYNATECH RESEARCH & DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/1977
Days to Decision
11 days