Hoveround Corp.
Hoveround Corp. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2013.
Top product codes for Hoveround Corp.
Recent clearances by Hoveround Corp.
- K122707 — HOVERROUND TEKNIQUE
- K122741 — HOVEROUND TEKNIQUE
- K100527 — HOVEROUND TEKNIQUE, MODEL HD-6
- K093946 — HOVEROUND HOVERGLIDE MODEL HOVERGLIDE MK-2
- K100350 — HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT
- K090108 — HOVEROUND TEKNIQUE FWD MK4 POWER WHEELCHAIR
- K042920 — HOVEROUND SE-3 POWERCHAIR
- K043069 — HOVEROUND E100 POWER CHAIR
- K042545 — HOVEROUND MPV-5 POWERCHAIR
- K042033 — HOVEROUND POWER WHEELCHAIR, MODEL HD700
- K022993 — HOVEROUND REHAB SEATING SYSTEM FOR POWER WHEELCHAIRS
- K021136 — TEKNIQUE-HOVEROUND POWER WHEEL CHAIR
- K010075 — TEKNIQUE
- K991132 — ACTIVA
- K954131 — HOVEROUND POWER WHEELCHAIR OR HVR-200 BY HOVEROUND
- K932329 — HOVEROUND POWER CHAIR
- K935410 — HOVEROUND MPV
Data sourced from openFDA. This site is unofficial and independent of the FDA.