Last synced on 25 January 2026 at 3:41 am

STERITEC INTEGRAPH MODEL CI-101

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960441
510(k) Type
Traditional
Applicant
Steritec Products Mfg Co, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1997
Days to Decision
462 days
Submission Type
Summary

STERITEC INTEGRAPH MODEL CI-101

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960441
510(k) Type
Traditional
Applicant
Steritec Products Mfg Co, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1997
Days to Decision
462 days
Submission Type
Summary