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CHEST FLUID MONITOR

Page Type
Cleared 510(K)
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)
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