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(1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250; (2) FULLY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL MD-700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990380
510(k) Type
Traditional
Applicant
MEDITEC CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/22/1999
Days to Decision
14 days
Submission Type
Summary

(1) DIGITAL BLOOD PRESSURE MONITOR, MODEL MD-250; (2) FULLY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL MD-700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990380
510(k) Type
Traditional
Applicant
MEDITEC CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/22/1999
Days to Decision
14 days
Submission Type
Summary