Last synced on 14 November 2025 at 11:06 pm

FLEXILOG 2000

Page Type
Cleared 510(K)
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)
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