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STERITEC INTEGRAPH MODEL CI-101

Page Type
Cleared 510(K)
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)
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