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DUO-MAX BLOOD PRESSURE & GLUCOSE MONITOR HMF-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080636
510(k) Type
Traditional
Applicant
HUBDIC CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2009
Days to Decision
344 days
Submission Type
Summary

DUO-MAX BLOOD PRESSURE & GLUCOSE MONITOR HMF-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080636
510(k) Type
Traditional
Applicant
HUBDIC CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2009
Days to Decision
344 days
Submission Type
Summary