STIMUPLEX, NERVE STIMULATOR
FDA 510(k) clearance K860126 · decided 1986-02-28
Clearance details
- K-number
- K860126
- Device name
- STIMUPLEX, NERVE STIMULATOR
- Applicant
- Burron Medical Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-01-14
- Decision date
- 1986-02-28
- Days to decision
- 45 days
- Clearance type
- Traditional
- Product code
- BXN
- Device class
- 2
- Regulation number
- 868.2775
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Bethlehem, PA, US
- Third-party review
- No
- Expedited review
- No
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Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| STIMPOD NMS450 Nerve Stimulator (K213049) | Xavant Technology (Pty), Ltd. | 2022-10-16 |
| MultiStim ECO (K162086) | PAJUNK GmbH Medizintechnologie | 2017-01-06 |
| SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve Stimulator (K153045) | Easy Med Instrument Co., Ltd. | 2016-05-13 |
| MiniStim MS-IVB Peripheral Nerve Stimulator (K143095) | Halyard Health, Inc. | 2015-03-24 |
| STIMPOD ST2-3010 NERVE STIMULATOR (K140853) | Xavant Technology (Pty), Ltd. | 2014-11-06 |
| EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN (K121743) | Sunmed, LLC | 2013-03-28 |
| MYOGUIDE SYSTEM MODEL 8008 (K111985) | Intronix Technologies Corp. | 2011-12-30 |
| STIMTRODE SINGLE USE NERVE STIMULATOR (K110118) | Xavant Technology (Pty), Ltd. | 2011-02-17 |
| STIMPOD NMS450 NERVE STIMULATOR (K102084) | Xavant Technology (Pty), Ltd. | 2010-12-16 |
| STIMPOD MODEL NMS-400 NERVE STIMULATOR (K093591) | Xavant Technology (Pty), Ltd. | 2009-12-03 |
| ASCEND (K091155) | Neurometrix, Inc. | 2009-09-03 |
| XPOD/XMAP NERVE STIMULATOR (K072092) | Xavant Technology (Pty), Ltd. | 2007-11-15 |
Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251. recall (Z-2131-2024) | B Braun Medical Inc | 2024-06-11 |
| Stimuplex A, 30 DEG, 21GX4", 0.80x100mm, Catalogue Number: 4894260 recall (Z-2132-2024) | B Braun Medical Inc | 2024-06-11 |
| Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278 recall (Z-2133-2024) | B Braun Medical Inc | 2024-06-11 |
| Stimuplex A, 30 DEG, 22GX2", 0.70x50mm, Catalogue Number: 4894502 recall (Z-2134-2024) | B Braun Medical Inc | 2024-06-11 |