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IOSERT LENS IMPLANT INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K854197
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1986
Days to Decision
99 days

IOSERT LENS IMPLANT INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K854197
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1986
Days to Decision
99 days