← Back to catalogue

Spark

FDA UDI

Class I (US FDA UDI)

by Ki Mobility, Llc

Identity

Trade Name
SPARK FDA UDI
Generic Name
Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name
SPARK MANUAL WHEELCHAIR FDA UDI
Model / Reference
SPARK FDA UDI
Description
SPARK MANUAL WHEELCHAIR FDA UDI

Identifiers

Primary DI / UDI-DI
00850013379040 FDA UDI
510(k) Number
K223527 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Push-rim manual wheelchair, non-bariatric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

Yes

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

Yes

FDA UDI

Category: Push-rim manual wheelchair, non-bariatric

Spark by Ki Mobility, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Push-rim manual wheelchair, non-bariatric.

Cleared under the same submission

K223527 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
Ki Mobility, Llc

Sources (1)

  • FDA UDI 633fe6d5-e284-47d8-a9b9-9b33077524c5 35 fields · synced Jun 1, 2026