FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HOVEROUND SE-3 POWERCHAIR

K Number: K042920 · Decision Dec 3, 2004
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
17
Review Days
42

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Basic Information

Device Name
HOVEROUND SE-3 POWERCHAIR
K Number
K042920
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hoveround Corp.
Date Received
October 22, 2004
Decision Date
December 3, 2004
Product Code
ITI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ITI Wheelchair, Powered

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Other Clearances by Hoveround Corp.

K Number Device Name
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
K043069 HOVEROUND E100 POWER CHAIR
K042545 HOVEROUND MPV-5 POWERCHAIR
K042033 HOVEROUND POWER WHEELCHAIR, MODEL HD700
K022993 HOVEROUND REHAB SEATING SYSTEM FOR POWER WHEELCHAIRS
Search all 17 clearances from Hoveround Corp. →