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DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881003
510(k) Type
Traditional
Applicant
HEALTHCHECK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1988
Days to Decision
70 days

DIGITAL BLOOD PRESSURE MONITOR MODEL CX-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881003
510(k) Type
Traditional
Applicant
HEALTHCHECK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1988
Days to Decision
70 days