Last synced on 25 January 2026 at 3:41 am

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003533
510(k) Type
Abbreviated
Applicant
Steritec Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2001
Days to Decision
83 days
Submission Type
Statement

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003533
510(k) Type
Abbreviated
Applicant
Steritec Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2001
Days to Decision
83 days
Submission Type
Statement