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EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-200M/HD-200

Page Type
Cleared 510(K)
510(k) Number
K021240
510(k) Type
Traditional
Applicant
Eikon Healthcare Device Corp.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
11/8/2002
Days to Decision
204 days
Submission Type
Statement

EIKON AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-200M/HD-200

Page Type
Cleared 510(K)
510(k) Number
K021240
510(k) Type
Traditional
Applicant
Eikon Healthcare Device Corp.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
11/8/2002
Days to Decision
204 days
Submission Type
Statement