Product code LQW
- Device name
- Test, Temperature Discrimination
- Medical specialty
- Neurology
- Device class
- 1
- Regulation number
- 882.1200
- Review panel
- NE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
Related GUDID Devices#
| Primary DI | Brand | Company | Published |
|---|---|---|---|
| 00850071298390 | Monofilament Set | Hyperion Medical Technologies, Inc. | 2026-06-02 |
| 00850071298383 | STX4 | Hyperion Medical Technologies, Inc. | 2026-06-02 |
| 08908022363016 | NEURO TOUCH | YOSTRA LABS PRIVATE LIMITED | 2024-01-10 |
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