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DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181

Page Type
Cleared 510(K)
510(k) Number
K993890
510(k) Type
Traditional
Applicant
NIHON SEIMITSU SOKKI CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1999
Days to Decision
15 days
Submission Type
Summary

DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181

Page Type
Cleared 510(K)
510(k) Number
K993890
510(k) Type
Traditional
Applicant
NIHON SEIMITSU SOKKI CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1999
Days to Decision
15 days
Submission Type
Summary