American Laser Medical
Salt Lake City, UT, US
American Laser Medical appears in FDA device records in Salt Lake City, UT. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for American Laser Medical between 1996 and 1999. The busiest year on record is 1997, with 3. The most recent is 1999, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1996 | 1 |
| 1997 | 3 |
| 1999 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K990780 | NUVOLASE 532 CUTANEOUS LASER SYSTEM | GEX | Substantially Equivalent | |
| K972765 | NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER | GEX | Substantially Equivalent | |
| K972561 | NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY | GEX | Substantially Equivalent | |
| K970667 | NUVO-LASE 660 LASER SYSTEM | GEX | Substantially Equivalent | |
| K963389 | FLEX-LASE 600 SERIES ION LASER SYSTEM | GEX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain