510(k) DEN130018 ยท PFX System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection
CYTOSCAN(R) DX
| Applicant | Affymetrix, Inc., Santa Clara CA, US |
| Decision | Unknown, Jan 17, 2014 |
| Received | Dec 18, 2013 |
| Type | Post-NSE |
| FDA record | Open on fda.gov |
Recalls that name DEN130018
No recall in the FDA data names this 510(k).
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