HOBBS MEDICAL CLEANING BRUSH— 510(k) K933354

Name: FDA 510(k) clearance K933354
Creator: U.S. Food and Drug Administration
Published: 1993-10-28

Substantially Equivalent

Hobbs Medical, Inc.

FDA 510(k) clearance K933354 for HOBBS MEDICAL CLEANING BRUSH, Substantially Equivalent on 1993-10-28. Applicant: Hobbs Medical, Inc.. Device class: 2.

Clearance details

Applicant: Hobbs Medical, Inc.
Product code: Code FEB
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-07-09
Decision date: 1993-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palmer, MA, US

Download summary PDF View 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, 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.