QuickPlan

510(k) K151560

QuickPlan is a medical device (FDA Class II; FDA product code MUJ, System, Planning, Radiation Therapy Treatment) made by Siris Medical, cleared under FDA 510(k) K151560 on 11 Sep 2015, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K151560↗

FDA record

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK151560	Date11 Sep 2015Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K151560

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K151560
FDA product code: MUJ

Device class: Class II
Regulation: 21 CFR Part 892.5050
Advisory committee: Radiology
FDA decision: SESE Substantially Equivalent

Devices cleared under K151560

2 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K151560
		UDI-DI	Size and differences
InsightRT CDS IRT100 Siris Medical	IRT100 / IRT100	B244IRT1000	—	On the market
InsightRT Software Suite Server ISS100S Siris Medical	ISS100S / ISS100S	B244ISS100S0	—	No longer on the market

Similar devices

Other devices filed under FDA product code MUJ (System, Planning, Radiation Therapy Treatment).

Other devices from Siris Medical

InsightRT CDS IRT100

Class II