# K973290: Syntec True Light Endoillumiinator with Pick

- Pathway: 510(k) (Traditional)
- Applicant: Vaughan Weeks
- Decided: Nov 14, 1997 after 73 days
- Product code: MPA (Endoilluminator)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K875004 (1988). 1 ancestor in all.
1 later device descends 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)
- K875004: Prisma Dispos. Brite Lite Fiberoptic Endo. W/Pick, Advanced Surgical Products, Inc. (1988) Summary page 1.
- (no number) Gamp & Associates Disposable Fiberoptic Endoilluminator with Pick: named in the summary without a submission number

## Most influential descendants
- K202670: Nam illumination probe with chopper (2021), 0 descendants of its own

## Indications for use
The Syntec, Inc. True Light Endoilluminator with Pick is used to illuminate with visible spectrum light the intra ocular portion of the eye for improved visualization and manipulation during vitreo-retinal surgery.

Source page: https://510kreport.com/device/K973290
Methodology: https://510kreport.com/methodology