# K932832: Primus Insulated Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Marlo Surgical Technology
- Decided: Feb 25, 1994 after 261 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- 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; 1 cites 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021237: Coopersurgical Laparoscopic Instruments (2003), 11 descendants of its own
- K043013: Miltex Laparoscopic Instruments (2005), 10 descendants of its own
- K052759: Dan Monopolar Lap Accessories (2006), 8 descendants of its own
- K081503: Aed Monopolar Lap Accessories (2008), 7 descendants of its own
- K103508: Unmiax Laparoscopic Instrument (2011), 6 descendants of its own

Source page: https://510kreport.com/device/K932832
Methodology: https://510kreport.com/methodology