HHP

2 FDA 510(k) clearances · Product code

FDA profile

Official device name

Table, Obstetrical, Manual (And Accessories)

Device class

Class II (moderate risk)

Regulation

21 CFR 884.4900

Medical specialty

Obstetrics/Gynecology

Adverse events (MAUDE)

1994: 1 · 1998: 2 · 1999: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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