AED RESECTOSCOPE— 510(k) K102663
Substantially EquivalentNational Advanced Endoscopy Devices, Inc.
FDA 510(k) clearance K102663 for AED RESECTOSCOPE, Substantially Equivalent on 2010-12-30. Applicant: National Advanced Endoscopy Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- National Advanced Endoscopy Devices, Inc.
- Product code
- Code FJL
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Canoga Park, CA, US
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More clearances from National Advanced Endoscopy Devices, Inc.
view allAdverse events under product code FJL
product code FJL- Death
- 2
- Total
- 2
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.