FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM

K Number: K896288 · Decision May 4, 1990
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
48
Applicant Total
8
Review Days
186

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Basic Information

Device Name
FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM
K Number
K896288
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1400
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Oakfield Instruments, Ltd.
Date Received
October 30, 1989
Decision Date
May 4, 1990
Product Code
FFT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FFT Electrode, Ph, Stomach

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FFT), ordered by most recent decision date.

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Other Clearances by Oakfield Instruments, Ltd.

K Number Device Name
K964804 FLEXILOG LS
K964589 FLEXILOG 3000
K961895 FLEXILOG LS 13921
K945069 FLEXILOG 2000
K920115 MEDISCINT
K902460 CARDIOSCINT (LEFT VENTRICULAR FUNCTION MONITOR)
K894902 SOURCERER