Laserguide
Laserguide appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 22, 1988.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K880071 | SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE | March 22, 1988 |
| K875104 | SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USE | February 2, 1988 |
| K873892 | SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE | February 2, 1988 |
| K873664 | LIGHT-SPOT FIBEROPTIC LASER HANDPIECE | November 6, 1987 |
| K873571 | LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBE | November 6, 1987 |