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MODIFIED SITE MACROBORE PHACO NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K922595
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1992
Days to Decision
90 days
Submission Type
Summary

MODIFIED SITE MACROBORE PHACO NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K922595
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1992
Days to Decision
90 days
Submission Type
Summary