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ULTRASPHYG BLOOD PRESSURE OPTION

Page Type
Cleared 510(K)
510(k) Number
K780046
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1978
Days to Decision
65 days

ULTRASPHYG BLOOD PRESSURE OPTION

Page Type
Cleared 510(K)
510(k) Number
K780046
510(k) Type
Traditional
Applicant
CAVITRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1978
Days to Decision
65 days