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STERILIZER, SERIES 3000, MODIFICATION TO

Page Type
Cleared 510(K)
510(k) Number
K770682
510(k) Type
Traditional
Applicant
CASTLE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1977
Days to Decision
39 days

STERILIZER, SERIES 3000, MODIFICATION TO

Page Type
Cleared 510(K)
510(k) Number
K770682
510(k) Type
Traditional
Applicant
CASTLE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1977
Days to Decision
39 days