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BP50 BLOOD PRESSURE AND PULSE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901392
510(k) Type
Traditional
Applicant
PULSE TIME PRODUCTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/23/1990
Days to Decision
150 days

BP50 BLOOD PRESSURE AND PULSE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901392
510(k) Type
Traditional
Applicant
PULSE TIME PRODUCTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/23/1990
Days to Decision
150 days