DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.— 510(k) K864956
Substantially EquivalentLa Jolla Technology, Inc.
FDA 510(k) clearance K864956 for DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA., Substantially Equivalent on 1987-03-09. Applicant: La Jolla Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- La Jolla Technology, Inc.
- Product code
- Code GZJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code GZJ
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