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AMP PORTABLE PATIENT PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K802600
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
22 days

AMP PORTABLE PATIENT PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K802600
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1980
Days to Decision
22 days