Lasermatic, Inc.
Finland, FI
Lasermatic, Inc. appears in FDA device records in Finland, FI. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Lasermatic, Inc. between 1988 and 1991. The busiest year on record is 1988, with 6. The most recent is 1991, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 6 |
| 1989 | 2 |
| 1990 | 1 |
| 1991 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K903131 | LASERMATIC SUPERCOMBO(TM) SURGICAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K901638 | MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33 | GEX | Substantially Equivalent | |
| K895279 | LASERMATIC COMBOLASER MODEL 5050 | GEX | Substantially Equivalent | |
| K893529 | COMBOLASER MODEL 5050 | GEX | Substantially Equivalent | |
| K871875 | MODEL 5050 SURGILASER FOR OB-GYN USE | HHR | Substantially Equivalent | |
| K870587 | LASERMATIC SURGILASER MODEL 5050 | EWG | Substantially Equivalent for Some Indications | |
| K871934 | MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE | LNK | Substantially Equivalent | |
| K871932 | MODEL 5050 SURGILASER FOR UROLOGY USE | LNK | Substantially Equivalent | |
| K871933 | MODEL 5050 SURGILASER FOR NEUROSURGERY USE | GEX | Substantially Equivalent | |
| K871876 | MODEL 5050 SURGILASER FOR PULMONARY USE | LLO | 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