← Back to catalogue

Modular Power Positioning System

FDA UDI

Class II (US FDA UDI)

by Motion Concepts Inc

Identity

Trade Name
MODULAR POWER POSITIONING SYSTEM FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Device Name
REHAB/CAPTAIN SEAT with 12" Lift FDA UDI
Model / Reference
RS-12L-MAXX FDA UDI
Description
REHAB/CAPTAIN SEAT with 12" Lift FDA UDI

Identifiers

Primary DI / UDI-DI
07540147011024 FDA UDI
510(k) Number
K150574 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electric-motor-driven wheelchair, occupant-controlled

Modular Power Positioning System by Motion Concepts Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric-motor-driven wheelchair, occupant-controlled.

Cleared under the same submission

K150574 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Motion Concepts Inc

Sources (1)

  • FDA UDI 711967a2-5b8d-4b46-beea-ab8cba119196 35 fields · synced May 29, 2026