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MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872144
510(k) Type
Traditional
Applicant
VESTRA-SUBCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1987
Days to Decision
55 days

MODIFIED DIGITAL BLOOD PRESSURE/PULSE METER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872144
510(k) Type
Traditional
Applicant
VESTRA-SUBCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1987
Days to Decision
55 days