# K081760: RSVP Phantom Pelvis, Model TLP260

- Pathway: 510(k) (Traditional)
- Applicant: The Phantom Laboratory, Inc.
- Decided: Jul 29, 2008 after 39 days
- Product code: IYE (Accelerator, Linear, Medical)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K954634 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954634: Radiosurgery Verification Phantom, The Phantom Laboratory, Inc. (1995) Summary page 1.

## Indications for use
The RSVP PhantomTM Pelvis is designed for use in a variety of radiation therapy applications including, final quality verification of therapy dose delivery and for comparing the delivered dose profiles for different treatment plans. It is also used for periodic quality assurance evaluations and acceptance testing and to perform reevaluations after equipment or software upgrades.

Source page: https://510kreport.com/device/K081760
Methodology: https://510kreport.com/methodology