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FLEXILOG LS

Page Type
Cleared 510(K)
510(k) Number
K964804
510(k) Type
Traditional
Applicant
Oakfield Instruments, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
250 days
Submission Type
Summary

FLEXILOG LS

Page Type
Cleared 510(K)
510(k) Number
K964804
510(k) Type
Traditional
Applicant
Oakfield Instruments, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/6/1997
Days to Decision
250 days
Submission Type
Summary