The Laryngeal Mask Co., Ltd.
San Diego, CA, US
The Laryngeal Mask Co., Ltd. appears in FDA device records in San Diego, CA. FDA records list 4 510(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
- 4
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 4 510(k) clearances for The Laryngeal Mask Co., Ltd. between 2000 and 2014. The busiest year on record is 2000, with 1. The most recent is 2014, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 1 |
| 2005 | 1 |
| 2007 | 1 |
| 2014 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K130304 | LMA FAMILY OF AIRWAYS | CAE | Substantially Equivalent | |
| K062475 | LMA STONEBREAKER DEVICE; PROBE SIZE 1.0MM, 1.6MM, 2.0MM | FFK | Substantially Equivalent | |
| K051993 | LMA FASTRACH ETT SINGLE USE | BTR | Substantially Equivalent | |
| K991580 | ILM ENDOTRACHEAL TUBE | BTR | 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