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BLOOD PRESSURE DEVICE, 400 SERIES

Page Type
Cleared 510(K)
510(k) Number
K781906
510(k) Type
Traditional
Applicant
MED-TEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1978
Days to Decision
3 days

BLOOD PRESSURE DEVICE, 400 SERIES

Page Type
Cleared 510(K)
510(k) Number
K781906
510(k) Type
Traditional
Applicant
MED-TEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1978
Days to Decision
3 days