'EXMOOR' SINGLE USE SUCTION TUBE— 510(k) K892504

Substantially Equivalent

Exmoor Plastics , Ltd.

FDA 510(k) clearance K892504 for 'EXMOOR' SINGLE USE SUCTION TUBE, Substantially Equivalent on 1989-06-22. Applicant: Exmoor Plastics , Ltd..

Clearance details

Applicant: Exmoor Plastics , Ltd.
Product code: Code LRC
Advisory panel: Ear, Nose, Throat
Date received: 1989-04-11
Decision date: 1989-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taunton, GB

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Adverse events under product code LRC

product code LRC

Death: 5
Total: 5

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.