MEDIVATORS ADVANTAGE PLUS ENDOSCOPE REPROCESSING SYSTEM, RAPICIDE PA HIGH LEVEL DISINFECTANT— 510(k) K082988

Substantially Equivalent

Medivators Reprocessing Systems

FDA 510(k) clearance K082988 for MEDIVATORS ADVANTAGE PLUS ENDOSCOPE REPROCESSING SYSTEM, RAPICIDE PA HIGH LEVEL DISINFECTANT, Substantially Equivalent on 2009-02-13. Applicant: Medivators Reprocessing Systems. Device class: 2.

Clearance details

Applicant
Medivators Reprocessing Systems
Product code
Code FEB
Device class
Class 2
Regulation
21 CFR 876.1500
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Minneapolis, MN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FEB

product code FEB
Malfunction
3,879
Total
3,879

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K082988

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K082988.

Data sourced from openFDA. This site is unofficial and independent of the FDA.