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

THE LIBERATOR WHEELCHAIR

K Number: K010859 · Decision Apr 5, 2001
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
2
Review Days
14

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THE LIBERATOR WHEELCHAIR
K Number
K010859
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Liberator Wheelchairs, Inc.
Date Received
March 22, 2001
Decision Date
April 5, 2001
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.

View all

Other Clearances by Liberator Wheelchairs, Inc.

K Number Device Name
K984391 THE LIBERATOR