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Monitor, Esophageal Motility, Anorectal Motility, And Tube
FDA product code KLA · Class 2 · Gastroenterology, Urology
541
Registered devices
7
Adverse events
1
Recalls
31
510(k) clearances
Devices with this code
SOLAR Anorectal Manometry Catheter — Laborie Medical Technologies Corp.Mui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises IncMui Scientific — H & A Mui Enterprises Inc
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-04-06 | Medtronic Gastroenterology / Urology | Mislabeling- The 8 ports of the manometric catheter were incorrectly labeled 1,3,5,7,8,2,4,6 from the distal to the proximal end of the catheter. The correct p |
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