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MOVABLE CORE SAFETY GUIDE

Page Type
Cleared 510(K)
510(k) Number
K790258
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1979
Days to Decision
17 days

MOVABLE CORE SAFETY GUIDE

Page Type
Cleared 510(K)
510(k) Number
K790258
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1979
Days to Decision
17 days