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DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF

Page Type
Cleared 510(K)
510(k) Number
K896788
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
46 days

DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF

Page Type
Cleared 510(K)
510(k) Number
K896788
510(k) Type
Traditional
Applicant
ADVANCED MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
46 days