Last synced on 25 January 2026 at 3:41 am

CROSS-CHECKS DUAL, MODEL CI 125

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010534
510(k) Type
Traditional
Applicant
Steritec Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
164 days
Submission Type
Statement

CROSS-CHECKS DUAL, MODEL CI 125

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010534
510(k) Type
Traditional
Applicant
Steritec Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
164 days
Submission Type
Statement