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BLOOD PRESSURE MONITOR, MODEL KP-7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032492
510(k) Type
Special
Applicant
K-JUMP HEALTH CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2003
Days to Decision
28 days
Submission Type
Summary

BLOOD PRESSURE MONITOR, MODEL KP-7000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032492
510(k) Type
Special
Applicant
K-JUMP HEALTH CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2003
Days to Decision
28 days
Submission Type
Summary