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THE 500 MONITOR SERIES

Page Type
Cleared 510(K)
510(k) Number
K823052
510(k) Type
Traditional
Applicant
VITATEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1982
Days to Decision
43 days

THE 500 MONITOR SERIES

Page Type
Cleared 510(K)
510(k) Number
K823052
510(k) Type
Traditional
Applicant
VITATEK
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/1982
Days to Decision
43 days