Alpha Source Battery AS35943

by Alpha Source Inc.

Alpha Source Battery AS35943 is a Class III device made by Alpha Source Inc., cleared under FDA 510(k) K032051 on 9 Jan 2004 and listed in FDA GUDID since 1 Jul 2019 (UDI-DI 00814314011627), active as of 22 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 22 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00814314011627 UDI-DI	Date1 Jul 2019Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK032051	Date9 Jan 2004Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00814314011627
FDA 510(k) database 510(k) number K032051

Across registries

2 registries list this device

FDA 510(k) K032051 decided 9 Jan 2004 Active
FDA GUDID UDI-DI 00814314011627 listed 1 Jul 2019 Listed

Timeline

2 dated events

9 Jan 2004 Cleared FDA 510(k) K032051
1 Jul 2019 Listed FDA GUDID 00814314011627

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Alpha Source Battery
Generic name: Portable/mobile rechargeable battery pack
Model / Ref / Catalog: AS35943

Primary DI / UDI-DI: 00814314011627
510(k) Number: K032051
FDA product code: MKJ
GMDN term: Portable/mobile rechargeable battery pack

Device class: Class III
Regulation number: 870.5310
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Portable/mobile rechargeable battery pack.

Other devices from Alpha Source Inc.

See all devices from Alpha Source Inc. →

Properties

Prescription use
Lot / batch number
Expiration date
Manufacturing date

Other properties (11, all answered No)