Last synced on 18 April 2025 at 11:05 pm

STERILIZER, SERIES 3000, MODIFICATION TO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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