TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050— 510(k) K033188
Substantially EquivalentIdev Technologies, Inc.
FDA 510(k) clearance K033188 for TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050, Substantially Equivalent on 2003-11-19. Applicant: Idev Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Idev Technologies, Inc.
- Product code
- Code MMX
- Device class
- Class 2
- Regulation
- 21 CFR 870.5150
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Houston, TX, US
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Adverse events under product code MMX
product code MMX- Death
- 3
- Total
- 3
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.