# K913365: Accuscope (TM) & Accuscope II (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Vineland Medical Products, Inc.
- Decided: Apr 27, 1992 after 273 days
- Product code: HEX (Colposcope (And Colpomicroscope))
- Device class: 2
- Regulation: 21 CFR 884.1630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K031639: Intermed Zoom Colposcope (2003), 2 descendants of its own
- K132423: The Gynocular (2014), 0 descendants of its own
- K073053: Colpo-Master (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K913365
Methodology: https://510kreport.com/methodology