American Laser Corp.
American Laser Corp. 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 April 5, 2001.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K010046 | NUVOLASE 532 MEDICAL LASER SYSTEM | April 5, 2001 |
| K990665 | BQ/BM INTEGRATED LASER DELIVERY SYSTEM | May 17, 1999 |
| K990725 | NUVOLASE 532 LASER SYSTEM | March 22, 1999 |
| K827819 | LASER PHOTOCOAGULATOR | January 7, 1983 |
| K813429 | LASER PHOTOCOAGULATOR ARGON MED. LASER | January 22, 1982 |