Last synced on 18 April 2025 at 11:05 pm

MODEL FB-20 NON-INVASIVE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861504
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
124 days

MODEL FB-20 NON-INVASIVE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861504
510(k) Type
Traditional
Applicant
FUKUDA DENSHI USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
124 days