# K952672: Vertical Integrated Perfect View (Vip) Radiographic System

- Pathway: 510(k) (Traditional)
- Applicant: Bennett X-Ray Corp.
- Decided: Jul 13, 1995 after 31 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K022667: Hcmi X-Ray (2002), 0 descendants of its own
- K022737: Hcmi X-Ray High Requency Chiropractic Radiographic (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K952672
Methodology: https://510kreport.com/methodology