NEURO SECTOR FIXATION DEVICE— 510(k) K833522
Substantially EquivalentAdvanced Technology Laboratories, Inc.
FDA 510(k) clearance K833522 for NEURO SECTOR FIXATION DEVICE, Substantially Equivalent on 1984-05-25. Applicant: Advanced Technology Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Advanced Technology Laboratories, Inc.
- Product code
- Code GXW
- Device class
- Class 2
- Regulation
- 21 CFR 882.1240
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Recent devices under product code GXW
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