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FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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