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ABD Device
AQUILA BIOSCIENCE LIMITED · Model ABD-S0002 · UDI-DI 05391540450079
2
510(k) clearances
15
Adverse events
1
Recalls
14
Facilities
Description
ABD Device Emergency response against harmful bacteria & viruses Non-Toxic Decontamination for use on Skin
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-24 | Emergent Protective Products USA Inc | Complaints of leaking packets were received. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.