FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LEGEND (MANUAL WHEELCHAIR)

K Number: K934236 · Decision Mar 17, 1994
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
458
Applicant Total
3
Review Days
210

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Basic Information

Device Name
LEGEND (MANUAL WHEELCHAIR)
K Number
K934236
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fortress Lite-Style Wheelchairs, Inc.
Date Received
August 19, 1993
Decision Date
March 17, 1994
Product Code
IOR
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
IOR Wheelchair, Mechanical

Similar 510(k) Clearances

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

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Other Clearances by Fortress Lite-Style Wheelchairs, Inc.

K Number Device Name
K934232 COMMUTER (MANUAL/POWER WHEELCLHAIR)
K934234 VISION (MANUAL WHEELCHAIR)