KEYFILL— 510(k) K872053

Name: FDA 510(k) clearance K872053
Creator: U.S. Food and Drug Administration
Published: 1987-07-01

Substantially Equivalent

Mayfield Instruments, Ltd.

FDA 510(k) clearance K872053 for KEYFILL, Substantially Equivalent on 1987-07-01. Applicant: Mayfield Instruments, Ltd.. Device class: 2.

Clearance details

Applicant: Mayfield Instruments, Ltd.
Product code: Code CAD
Device class: Class 2
Regulation: 21 CFR 868.5880
Advisory panel: Anesthesiology
Date received: 1987-06-01
Decision date: 1987-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, M5a3ja, CA

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

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.