EN-SNARE ENDOVASCULAR SNARE AND CATHETER— 510(k) K021606
Substantially EquivalentMedical Device Technologies, Inc.
FDA 510(k) clearance K021606 for EN-SNARE ENDOVASCULAR SNARE AND CATHETER, Substantially Equivalent on 2002-05-31. Applicant: Medical Device Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Device 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
- Gainesville, FL, US
Recent devices under product code MMX
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- K050873 — CANALIZER HYDROPHILIC GUIDE WIRE
- K043523 — INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE
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.