FDA Product Code
FDA Product Code QGH — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Neurology
- 21 CFR Citation
- 882.5940
510(k) Clearances — 9 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K192834 | MECTA Sigma | Mecta Corporation | 2020-04-26 | Special | PDF ↗ |
| K965070 | SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M. | Mecta Corp. | 1997-03-06 | Traditional | PDF ↗ |
| K960754 | SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M | Mecta Corp. | 1996-09-18 | Traditional | PDF ↗ |
| K945120 | THYMATRON 2000 ELECTROCONVULSIVE SYSTEM | Somatics, Inc. | 1995-10-26 | Traditional | PDF ↗ |
| K911144 | MF-500, MODIFICATION | Elcot, Inc. | 1991-10-18 | Traditional | PDF ↗ |
| K863815 | ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000 | Elcot, Inc. | 1987-06-02 | Traditional | PDF ↗ |
| K860467 | ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 | Medcraft Corp. | 1986-11-10 | Traditional | PDF ↗ |
| K852069 | MECTA ECT DEVICE MODELS SR & JR | Mecta Corp. | 1985-08-09 | Traditional | PDF ↗ |
| K843923 | THYMATRON | Somatics, Inc. | 1984-12-03 | Traditional | PDF ↗ |
Product code QGH · Class II · Neurology. Data: openFDA.