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OHMEDA 2350 FINAPRES(R) BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880572
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1988
Days to Decision
89 days

OHMEDA 2350 FINAPRES(R) BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880572
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1988
Days to Decision
89 days