LIGHT SABER INTRODUCER NEEDLE— 510(k) K013040

Substantially Equivalent

Minrad, Inc.

FDA 510(k) clearance K013040 for LIGHT SABER INTRODUCER NEEDLE, Substantially Equivalent on 2001-12-07. Applicant: Minrad, Inc..

Clearance details

Applicant: Minrad, Inc.
Product code: Code MDM
Advisory panel: General, Plastic Surgery
Date received: 2001-09-10
Decision date: 2001-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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Adverse events under product code MDM

product code MDM

Injury: 247
Malfunction: 1,516
Total: 1,763

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.