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Apron, Leaded

FDA product code EAJ · Class 1 · Radiology

8,795
Registered devices
114
Adverse events
25
Recalls
6
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could
2019-06-07Burlington Medical, LLCThe protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.