NES REPROCESSED VARICOSE VEIN RF CATHETER— 510(k) K090661
Substantially EquivalentNortheast Scientific, Inc.
FDA 510(k) clearance K090661 for NES REPROCESSED VARICOSE VEIN RF CATHETER, Substantially Equivalent on 2010-07-21. Applicant: Northeast Scientific, Inc.. Device class: 2.
Clearance details
- Applicant
- Northeast Scientific, Inc.
- Product code
- Code NUJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4400
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Waterbury, CT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.