ORAL BALANCE LIQUID/ GEL— 510(k) K061331

Substantially Equivalent

Laclede, Inc.

FDA 510(k) clearance K061331 for ORAL BALANCE LIQUID/ GEL, Substantially Equivalent on 2006-07-25. Applicant: Laclede, Inc..

Clearance details

Applicant: Laclede, Inc.
Product code: Code LFD
Advisory panel: Unknown
Date received: 2006-05-12
Decision date: 2006-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rancho Dominguez, CA, US

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Adverse events under product code LFD

product code LFD

Death: 3
Total: 3

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.