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FLEXILOG LS 13921

Page Type
Cleared 510(K)
510(k) Number
K961895
510(k) Type
Traditional
Applicant
Oakfield Instruments, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
172 days
Submission Type
Summary

FLEXILOG LS 13921

Page Type
Cleared 510(K)
510(k) Number
K961895
510(k) Type
Traditional
Applicant
Oakfield Instruments, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/4/1996
Days to Decision
172 days
Submission Type
Summary