A.R.C. Laser AG
A.R.C. Laser AG appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 1 compliance action on record. Its most recent 510(k) clearance was granted on Feb 8, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 1
- Compliance Actions
- 1
Known Names
A.R.C. Laser, A.R.C Laser
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K003512 | LASER PACK I, LASER PACK II, PHACO PACK I, PHACO PACK II | Feb 8, 2001 |
| K002986 | A.R.C. LOW BUBBLE TURBO NEEDLE, MODEL WE0106.5 | Nov 29, 2000 |
| K001511 | O-LAS OPHTHALMIC PHOTODISRUPTOR | Jul 19, 2000 |
| K993154 | LASER PHOTOLYSIS SYSTEM, PHARO OPHTHALMIC SURGERY SYSTEM | Jun 29, 2000 |