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HOME BLOOD PRESSURE KIT, ANEROID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884420
510(k) Type
Traditional
Applicant
YAMASU CO. LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/25/1989
Days to Decision
309 days

HOME BLOOD PRESSURE KIT, ANEROID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884420
510(k) Type
Traditional
Applicant
YAMASU CO. LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/25/1989
Days to Decision
309 days