HEADWAY 21 MICROCATHETER, MODEL: MC212150S— 510(k) K093160
Substantially EquivalentMicroVention, Inc.
FDA 510(k) clearance K093160 for HEADWAY 21 MICROCATHETER, MODEL: MC212150S, Substantially Equivalent on 2009-11-05. Applicant: MicroVention, Inc.. Device class: 2.
Clearance details
- Applicant
- MicroVention, Inc.
- Product code
- Code DQY
- Device class
- Class 2
- Regulation
- 21 CFR 870.1250
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Tistin, CA, US
Recent devices under product code DQY
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Adverse events under product code DQY
product code DQY- Death
- 464
- Injury
- 4,489
- Malfunction
- 13,721
- Other
- 2
- Total
- 18,676
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.