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FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896288
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/4/1990
Days to Decision
186 days

FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K896288
510(k) Type
Traditional
Applicant
OAKFIELD INSTRUMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/4/1990
Days to Decision
186 days