LYSOL I.C. BRAND INSTRUMENT DISINFECTANT PRESOAK— 510(k) K940383

Name: FDA 510(k) clearance K940383
Creator: U.S. Food and Drug Administration
Published: 1995-03-22

Substantially Equivalent

National Laboratories

FDA 510(k) clearance K940383 for LYSOL I.C. BRAND INSTRUMENT DISINFECTANT PRESOAK, Substantially Equivalent on 1995-03-22. Applicant: National Laboratories. Device class: 1.

Clearance details

Applicant: National Laboratories
Product code: Code LRJ
Device class: Class 1
Regulation: 21 CFR 880.6890
Advisory panel: General Hospital
Date received: 1994-01-26
Decision date: 1995-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montvale, NJ, US

Download summary PDF View on FDA.gov ↗

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More clearances from National Laboratories

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K940382 — LYSOL I.C. BRAND DISINFECTANT1995-04-21
K940381 — LYSOL I.C. BRAND QUATERNARY CLEANER DISINFECTANT1994-07-25

Adverse events under product code LRJ

product code LRJ

Injury: 958
Total: 958

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.