MB 102 MILLENNIUM BLADES— 510(k) K020122

Name: FDA 510(k) clearance K020122
Creator: U.S. Food and Drug Administration
Published: 2002-02-15

Substantially Equivalent

Millennium Biomedical, Inc.

FDA 510(k) clearance K020122 for MB 102 MILLENNIUM BLADES, Substantially Equivalent on 2002-02-15. Applicant: Millennium Biomedical, Inc.. Device class: 1.

Clearance details

Applicant: Millennium Biomedical, Inc.
Product code: Code HNO
Device class: Class 1
Regulation: 21 CFR 886.4370
Advisory panel: Ophthalmic
Date received: 2002-01-14
Decision date: 2002-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pomona, CA, US

Download summary PDF View on FDA.gov ↗

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K041110 — MB 105 MILLENNIUM BLADES2004-10-13
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Adverse events under product code HNO

product code HNO

Injury: 390
Total: 390

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.