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AHT INC

AHT INC · Model VD80 · UDI-DI 26975913450014

KZA
6
510(k) clearances
19
Adverse events
2
Recalls
28
Facilities

Recalls

DateFirmReason
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.
2012-03-14Christie Medical Holding IncInstrument may tip over if not moved correctly.

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Data 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.