SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI— 510(k) K926013

Name: FDA 510(k) clearance K926013
Creator: U.S. Food and Drug Administration
Published: 1993-02-12

Substantially Equivalent

Sporicidin Intl.

FDA 510(k) clearance K926013 for SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI, Substantially Equivalent on 1993-02-12. Applicant: Sporicidin Intl.. Device class: 1.

Clearance details

Applicant: Sporicidin Intl.
Product code: Code LRJ
Device class: Class 1
Regulation: 21 CFR 880.6890
Advisory panel: General Hospital
Date received: 1992-11-24
Decision date: 1993-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRJ

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K992661 — CONTROL III ELITE1999-09-14
K991509 — PRO-PORTION CLEANER/DISINFECTANT1999-07-14
K984485 — MICROSTAT 21999-01-13
K983947 — AMERSE 21998-12-04
K983869 — DISPATCH HOSPITAL CLEANER DISINFECTANT TOWELS WITH BLEACH1998-11-30

More clearances from Sporicidin Intl.

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K003087 — MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION2000-11-07
K983194 — SPORICIDIN STERILIZING AND DISINFECTING SOLUTION (SSDS)1999-03-05
K922262 — SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT1992-09-15
K904579 — SPORICIDIN BRAND DISINFECTANT TOWELETTES1992-05-18
K904580 — SPORICIDIN BRAND DISINFECTANT SPRAY1992-05-18

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.