# K914178: Corrected-V.P.S.

- Pathway: 510(k) (Traditional)
- Applicant: Jeneric/Pentron, Inc.
- Decided: Apr 28, 1992 after 223 days
- Product code: ELW (Material, Impression)
- Device class: 2
- Regulation: 21 CFR 872.3660
- Recalls of this device: 1 (0 Class I)
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K120013: Tempspan Clear Matrix (2012), 1 descendant of its own
- K132599: Smilebond System (2014), 0 descendants of its own

## Recalls of this device
- Nov 4, 2010 · Not classified · Z-1146-2012: Pentron Clinical is voluntarily recalling the following lot of mislabeled Correct VPS Medium Body Tubes. It was discovered that the individual tubes inside the Correct VPS Medium Body Tube boxes are m

Source page: https://510kreport.com/device/K914178
Methodology: https://510kreport.com/methodology