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MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901

Page Type
Cleared 510(K)
510(k) Number
K071384
510(k) Type
Traditional
Applicant
NIHON SEIMITSU SOKKI CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/9/2007
Days to Decision
145 days
Submission Type
Summary

MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901

Page Type
Cleared 510(K)
510(k) Number
K071384
510(k) Type
Traditional
Applicant
NIHON SEIMITSU SOKKI CO., LTD.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/9/2007
Days to Decision
145 days
Submission Type
Summary