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2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861987
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1987
Days to Decision
257 days

2120 NON-INVASIVE BLOOD PRESSURE MONITOR W/CUFF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861987
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1987
Days to Decision
257 days