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FLEXILOG 2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945069
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/13/1995
Days to Decision
242 days
Submission Type
Statement

FLEXILOG 2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945069
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/13/1995
Days to Decision
242 days
Submission Type
Statement