FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM— 510(k) K896288

Name: FDA 510(k) clearance K896288
Creator: U.S. Food and Drug Administration
Published: 1990-05-04

Substantially Equivalent

Oakfield Instruments, Ltd.

FDA 510(k) clearance K896288 for FLEXILOG 1010 AMBULATORY PH MONITORING SYSTEM, Substantially Equivalent on 1990-05-04. Applicant: Oakfield Instruments, Ltd.. Device class: 1.

Clearance details

Applicant: Oakfield Instruments, Ltd.
Product code: Code FFT
Device class: Class 1
Regulation: 21 CFR 876.1400
Advisory panel: Gastroenterology, Urology
Date received: 1989-10-30
Decision date: 1990-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oxon Ox8 1ja England, GB

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FFT

product code FFT

Injury: 595
Malfunction: 2,175
Other: 1
Total: 2,771

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.