# K942580: Neoprobe 1000 Portable Radioisotope Detector and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Neoprobe Corp.
- Decided: Feb 9, 1995 after 254 days
- Product code: IZD (Probe, Uptake, Nuclear)
- Device class: 1
- Regulation: 21 CFR 892.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K962319: Neoprobe 1000 Gen 1C Portable Radioisotope Detector & Accessories (1996), 4 descendants of its own
- K971167: Neoprobe Model 1500 Portable Radioisotope Detector and Accessories (1997), 3 descendants of its own
- K013751: Handheld Gamma Finder (HGF) (2002), 1 descendant of its own
- K101887: Confident Surgery Suite 300, Model CSS300 (2011), 0 descendants of its own
- K982442: C-Trak Automatic Analyzer (Name Change From Oncoprobe II to C-Trak) (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K942580
Methodology: https://510kreport.com/methodology