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MONITOR, NON-INVASIVE BLOOD PRESSURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K782000
510(k) Type
Traditional
Applicant
AUTOMATED SCREENING DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1978
Days to Decision
13 days

MONITOR, NON-INVASIVE BLOOD PRESSURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K782000
510(k) Type
Traditional
Applicant
AUTOMATED SCREENING DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1978
Days to Decision
13 days