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

COMMUTER (MANUAL/POWER WHEELCLHAIR)

K Number: K934232 · Decision Mar 29, 1994
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
3
Review Days
222

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Basic Information

Device Name
COMMUTER (MANUAL/POWER WHEELCLHAIR)
K Number
K934232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent for Some Indications
Applicant
Fortress Lite-Style Wheelchairs, Inc.
Date Received
August 19, 1993
Decision Date
March 29, 1994
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ITI), ordered by most recent decision date.

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Other Clearances by Fortress Lite-Style Wheelchairs, Inc.

K Number Device Name
K934234 VISION (MANUAL WHEELCHAIR)
K934236 LEGEND (MANUAL WHEELCHAIR)