LKW — Laser, Neurosurgical Class III
FDA Device Classification
Classification Details
- Product Code
- LKW
- Device Class
- Class III
- Regulation Number
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Unknown
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K875042 | surgilase | ND:YAG 100 SURGICAL LASER FOR NEURO & PULMONARY | June 24, 1988 |
| K880172 | cooper lasersonics | MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA. | March 11, 1988 |
| K864166 | weck surgical systems | 25 WATT CARBON DIOXIDE MEDICAL LASER FOR NEUROLOGY | February 10, 1987 |
| K853580 | endo lase | MEDILAS 2 | February 13, 1986 |
| K844440 | cooper lasersonics | MODEL 4000 ND:YAG LASER FOR HEMORRHAGE CONTROL | May 9, 1985 |