CONTROL III ELITE— 510(k) K992661

Substantially Equivalent

Maril Products, Inc.

FDA 510(k) clearance K992661 for CONTROL III ELITE, Substantially Equivalent on 1999-09-14. Applicant: Maril Products, Inc..

Clearance details

Applicant: Maril Products, Inc.
Product code: Code LRJ
Advisory panel: General Hospital
Date received: 1999-08-09
Decision date: 1999-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

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Adverse events under product code LRJ

product code LRJ

Injury: 958
Total: 958

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.