Medical Consultants Intl. , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K904264 | MODEL SW-103 SOLITANS STIMULATOR | May 9, 1991 |
| K900731 | MEDI LISS DENTAL ANALGESIA DEVICE (SBL601) | December 17, 1990 |
| K903654 | LISS CRANIAL STIMULATOR MODEL SBL202-B | October 4, 1990 |
| K902976 | MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC | September 7, 1990 |
| K894515 | LISS CRANIAL STIMULATOR MODEL SBL201-M | May 3, 1990 |
| K896226 | LISS BODY STIMULATOR MODEL SBL501-M | April 10, 1990 |