Arizona Oxygen Timer Device

by The John Bunn Co. 510(k)

Active United States

510(k) K761260

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK761260	Date16 Dec 1976Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K761260
FDA Product Code: BXP

Device Class: Class I
Regulation: 21 CFR Part 868.2885
Advisory Committee: Anesthesiology
FDA Decision: SESE Substantially Equivalent

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