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MONITOR, PULSE WAVE VELOCITY P607

Page Type
Cleared 510(K)
510(k) Number
K770330
510(k) Type
Traditional
Applicant
CYBORG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1977
Days to Decision
7 days

MONITOR, PULSE WAVE VELOCITY P607

Page Type
Cleared 510(K)
510(k) Number
K770330
510(k) Type
Traditional
Applicant
CYBORG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/1977
Days to Decision
7 days