LLF — Laser, Neurosurgical, Argon Class III
FDA Device Classification
Classification Details
- Product Code
- LLF
- 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 |
|---|
| K870773 | hgm | ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER | July 10, 1987 |
| K864610 | inframed | CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE | June 18, 1987 |
| K860977 | britt corp | MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION | October 16, 1986 |
| K833497 | cooper medical | COOPER MEDICAL MODEL 770 | April 17, 1984 |