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

ACTIVA

K Number: K991132 · Decision Oct 20, 1999
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
346
Applicant Total
17
Review Days
201

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Basic Information

Device Name
ACTIVA
K Number
K991132
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3800
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hoveround Corp.
Date Received
April 2, 1999
Decision Date
October 20, 1999
Product Code
INI
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
INI Vehicle, Motorized 3-Wheeled

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Other Clearances by Hoveround Corp.

K Number Device Name
K122707 HOVERROUND TEKNIQUE
K122741 HOVEROUND TEKNIQUE
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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
Search all 17 clearances from Hoveround Corp. →