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FLEXILOG 3000

Page Type
Cleared 510(K)
510(k) Number
K964589
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/4/1997
Days to Decision
109 days
Submission Type
Summary

FLEXILOG 3000

Page Type
Cleared 510(K)
510(k) Number
K964589
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/4/1997
Days to Decision
109 days
Submission Type
Summary