FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇹 Austria

Klaxon (Twist); Klaxon (Twist R)

K Number: K240267 · Decision Jan 10, 2025
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
2
Review Days
345

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
Klaxon (Twist); Klaxon (Twist R)
K Number
K240267
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Klaxon Mobility GmbH
Date Received
January 31, 2024
Decision Date
January 10, 2025
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 Klaxon Mobility GmbH

K Number Device Name
K222502 KLICK (VARIANTS: POWER, RACE, MONSTER)