CODE 17-ENDOSCOPE DEODORANT— 510(k) K840208

Substantially Equivalent

Knox Laboratories

FDA 510(k) clearance K840208 for CODE 17-ENDOSCOPE DEODORANT, Substantially Equivalent on 1984-07-19. Applicant: Knox Laboratories. Device class: 2.

Clearance details

Applicant
Knox Laboratories
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
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code FEB

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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 →

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