BAUSCH & LOMB RENU MULTI-PURPOSE SOLUTION— 510(k) K982775

Substantially Equivalent

Bausch & Lomb, Inc.

FDA 510(k) clearance K982775 for BAUSCH & LOMB RENU MULTI-PURPOSE SOLUTION, Substantially Equivalent on 1998-11-03. Applicant: Bausch & Lomb, Inc..

Clearance details

Applicant: Bausch & Lomb, Inc.
Product code: Code LPN
Advisory panel: Ophthalmic
Date received: 1998-08-07
Decision date: 1998-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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Adverse events under product code LPN

product code LPN

Injury: 333
Other: 8
Total: 341

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.