# K932669: Supra-Vit (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Medical Instrument Development Laboratories, Inc.
- Decided: Jun 3, 1994 after 366 days
- Product code: HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 3 cite it directly.
0 of 13 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
- K992943: Vit Enhancer (1999), 10 descendants of its own
- K020911: Mid Labs Autonomous Vit Enhancer (Ave) (2002), 9 descendants of its own
- K102222: Ultimate Vit Enhamcer (Uve) (2011), 8 descendants of its own
- K142877: EVA,anterior machine, EVA, combined machine, EVA combined machine with laser (DORC connector), EVA combined machine with laser SMA connector) (2015), 5 descendants of its own
- K190875: EVA, anterior machine, EVA, combined machine, EVA combined machine with laser (DORC connector), EVA combined machine with laser (SMA connector) (2019), 2 descendants of its own

Source page: https://510kreport.com/device/K932669
Methodology: https://510kreport.com/methodology