TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060— 510(k) K050926
Substantially EquivalentIdev Technologies, Inc.
FDA 510(k) clearance K050926 for TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060, Substantially Equivalent on 2005-05-09. 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
- Special
- Location
- Houston, TX, US
Recent devices under product code MMX
view allMore clearances from Idev Technologies, Inc.
view all- K130591 — SUPERA VERITAS
- K122546 — SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
- K111627 — SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
- K111766 — SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS
- K093893 — SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
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.