Atlas FDA

MCJ

1 FDA 510(k) clearances · Product code

FDA profile

Adverse events (MAUDE)
1992: 1 · 1993: 1 · 1994: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
NEOSERV 824 (K900729)Burdick Corp.1990-06-08

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Every clearance here is in the API, with alerts when new ones post.