Last synced on 18 April 2025 at 11:05 pm

SYSTEM 7100 NON-INVASIVE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897173
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1990
Days to Decision
300 days

SYSTEM 7100 NON-INVASIVE BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K897173
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/1990
Days to Decision
300 days