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LIBERATOR/STROLLER II SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K800742
510(k) Type
Traditional
Applicant
CRYOGENIC ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1980
Days to Decision
50 days

LIBERATOR/STROLLER II SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K800742
510(k) Type
Traditional
Applicant
CRYOGENIC ASSOC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/1980
Days to Decision
50 days