CAPHOSOL ARTIFICIAL SALIVA— 510(k) K991938

Substantially Equivalent

Inpharma A.S.

FDA 510(k) clearance K991938 for CAPHOSOL ARTIFICIAL SALIVA, Substantially Equivalent on 1999-08-10. Applicant: Inpharma A.S..

Clearance details

Applicant: Inpharma A.S.
Product code: Code LFD
Advisory panel: Unknown
Date received: 1999-06-09
Decision date: 1999-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northborough, MA, 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.