Lockheed-Martin Aculight
2 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Lockheed Martin Aculight Capella-r 1850 Laser. This device has the Accession number 061233 recall (Z-2069-2011) | Lockheed-Martin Aculight | 2011-05-19 |
| LM Aculight Corporation Perseus Pulsed Fiber Laser, Model number: ML36L-1541. Additional M recall (Z-1170-2010) | Lockheed-Martin Aculight | 2010-04-12 |
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Every clearance here is in the API, with alerts when new ones post.