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IOLAB/SITE PERISTALTIC MODULE

Page Type
Cleared 510(K)
510(k) Number
K944995
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1995
Days to Decision
358 days
Submission Type
Summary

IOLAB/SITE PERISTALTIC MODULE

Page Type
Cleared 510(K)
510(k) Number
K944995
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1995
Days to Decision
358 days
Submission Type
Summary