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DISP. NEONATAL BLOOD PRESSURE MONITORING CUFF

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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