SALINUM, ORCLAIR— 510(k) K024148

Substantially Equivalent

Sinclair Pharmaceuticals, Ltd.

FDA 510(k) clearance K024148 for SALINUM, ORCLAIR, Substantially Equivalent on 2003-09-15. Applicant: Sinclair Pharmaceuticals, Ltd..

Clearance details

Applicant: Sinclair Pharmaceuticals, Ltd.
Product code: Code LFD
Advisory panel: Unknown
Date received: 2002-12-16
Decision date: 2003-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Godalming, Surrey, GB

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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.