Medi Liss Dental Analgesia Device (SBL601)
FDA 510(k) K900731 · Medical Consultants Intl. , Ltd.
510(k) numberK900731
Submission
- Device name
- Medi Liss Dental Analgesia Device (SBL601)
- Applicant
- Medical Consultants Intl. , Ltd.
Glen Rock, NJ, US - Received
- February 15, 1990
- Decision date
- December 17, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LWM – Device, Electrical Dental Anesthesia
- Device class
- Unclassified
Other 510(k)s with product code LWM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K193570 | Dental Pain EraserLWM · Special | Synapse Dental | 01/17/2020SE |
| K192429 | Dental Pain EraserLWM · Traditional | Synapse Dental | 01/14/2020SE |
| K182947 | Dental Pain EraserLWM · Traditional | Synapse Dental, LLC | 03/26/2019SE |
| K011001 | Team-Up TM Dental Electronic Anesthesia SystemLWM · Traditional | Satelec | 06/07/2001SE |
| K935304 | 3M Dental Electronic Anesthesia (Dea) System 8670LWM · Traditional | 3M Company | 03/16/1994SE |
| K935085 | 3M Dental Electrononic Anesthesia (DEA0 System 8670 Additional ApplicationsLWM · Traditional | 3M Company | 01/26/1994SE |
| K935082 | 3M Dental Electronic Anesthesia (Dea) System 8670 ModificationLWM · Traditional | 3M Company | 01/26/1994SE |
| K915717 | CedetaLWM · Traditional | D-W Intl. | 11/23/1992SE |
| K920119 | 3M Dental Electronic Anesthesia SystemLWM · Traditional | 3M Company | 05/22/1992SE |
| K910625 | UltracalmLWM · Traditional | Sion Technology, Inc. | 05/15/1992SE |
More from Sion Technology, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K904264 | Model SW-103 Solitans StimulatorGZJ · Traditional | 05/09/1991SE |
| K903654 | Liss Cranial Stimulator Model SBL202-BQJQ · Traditional | 10/04/1990SE |
| K902976 | Medi Model SBL502-B (Liss Body Stimulator) Zero DCGZL · Traditional | 09/07/1990SE |
| K894515 | Liss Cranial Stimulator Model SBL201-MQJQ · Traditional | 05/03/1990SE |
| K896226 | Liss Body Stimulator Model SBL501-MGZJ · Traditional | 04/10/1990SE |
Questions and answers
When was Medi Liss Dental Analgesia Device (SBL601) cleared by the FDA?
Medi Liss Dental Analgesia Device (SBL601) (K900731) received a 510(k) decision of Substantially Equivalent on December 17, 1990, 305 days after the submission was received.
What is the product code of K900731?
The FDA product code is LWM – Device, Electrical Dental Anesthesia, a Unclassified device.