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ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR (0998-00-0117-XX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970061
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1997
Days to Decision
261 days
Submission Type
Statement

ACCUTORR PLUS NON INVASIVE BLOOD PRESSURE MONITOR (0998-00-0117-XX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970061
510(k) Type
Traditional
Applicant
DATASCOPE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1997
Days to Decision
261 days
Submission Type
Statement