NEUTRASAL— 510(k) K091718

Substantially Equivalent

Bartor Pharmacal Co., Inc.

FDA 510(k) clearance K091718 for NEUTRASAL, Substantially Equivalent on 2009-09-02. Applicant: Bartor Pharmacal Co., Inc..

Clearance details

Applicant: Bartor Pharmacal Co., Inc.
Product code: Code LFD
Advisory panel: Unknown
Date received: 2009-06-11
Decision date: 2009-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pomona, NY, US

Download summary PDF View on FDA.gov ↗

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.