510(k) K052872

IDOC UPPER ARM ATTACHED BLOOD PRESSURE AND PULSE RATE MONITOR, MODEL ID-42A/ID-43A by Taidoc Technology Corporation — Product Code DXN

K052872 is an FDA 510(k) premarket notification submitted by Taidoc Technology Corporation for the device "IDOC UPPER ARM ATTACHED BLOOD PRESSURE AND PULSE RATE MONITOR, MODEL ID-42A/ID-43A". The FDA issued a decision of Substantially Equivalent on Nov 23, 2005. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Taidoc Technology Corporation has 122 other 510(k) clearances on record.