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KERATOME SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K974243
510(k) Type
Traditional
Applicant
INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1998
Days to Decision
69 days
Submission Type
Summary

KERATOME SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K974243
510(k) Type
Traditional
Applicant
INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1998
Days to Decision
69 days
Submission Type
Summary