Scout RF 4-P

Scout RF 4-P (82554) is an electric-motor-driven wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Burke, Inc., cleared under FDA 510(k) K982158 on 31 Aug 1998 and listed in FDA GUDID since 1 Sep 2016 (UDI-DI B314825541), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB314825541 UDI-DI	Date1 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK982158	Date31 Aug 1998Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K982158

Across registries

2 registries list this device

FDA 510(k) K982158 decided 31 Aug 1998 Active
FDA GUDID UDI-DI B314825541 listed 1 Sep 2016 Listed

Timeline

2 dated events

31 Aug 1998 Cleared FDA 510(k) K982158
1 Sep 2016 Listed FDA GUDID B314825541

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Scout
Generic name: Electric-motor-driven wheelchair, occupant-controlled
Model / Ref / Catalog: RF 4-P, 82554

Primary DI / UDI-DI: B314825541
510(k) Number: K982158
FDA product code: ITI
GMDN term: Electric-motor-driven wheelchair, occupant-controlled

Device class: Class II
Regulation number: 890.3860
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Electric-motor-driven wheelchair, occupant-controlled.

Other devices from Burke, Inc.

See all devices from Burke, Inc. →

Properties

Serial number
Manufacturing date

Other properties (13, all answered No)