# Neoprobe Corp.

- Location (FDA's records): Dublin, OH
- FDA decisions: 6 (1986–2005): 6 510(k) clearances
- Product codes: IZD (5), DPW (1)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 5 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cardiosonix, Ltd.: 2 (https://510kreport.com/company/cardiosonix)
- Care Wise Medical Products Corp.: 1 (https://510kreport.com/company/care-wise-medical-products)
- Biosonix, Ltd.: 1 (https://510kreport.com/company/biosonix)
- Medi-Stim A/S: 1 (https://510kreport.com/company/medi-stim-a-s)
- Transonic Systems, Inc.: 1 (https://510kreport.com/company/transonic-systems)

## Firms that cite its devices most
- Care Wise Medical Products Corp.: 1 (https://510kreport.com/company/care-wise-medical-products)
- Surgiceye GmbH: 1 (https://510kreport.com/company/surgiceye)
- Silicon Instruments Gmhb: 1 (https://510kreport.com/company/silicon-instruments-gmhb)

## Its most-cited devices
- K971167: Neoprobe Model 1500 Portable Radioisotope Detector and Accessories (1997), cited by 3
- K942580: Neoprobe 1000 Portable Radioisotope Detector and Accessories (1995), cited by 1
- K962319: Neoprobe 1000 Gen 1C Portable Radioisotope Detector & Accessories (1996), cited by 1

## Recent decisions
- K050088: Quantix/or Blood Flow Monitor; Flexible Probe with Optional Vessel Stabilizer (Feb 8, 2005)
- K971167: Neoprobe Model 1500 Portable Radioisotope Detector and Accessories (Jun 26, 1997)
- K962319: Neoprobe 1000 Gen 1C Portable Radioisotope Detector & Accessories (Sep 13, 1996)
- K942580: Neoprobe 1000 Portable Radioisotope Detector and Accessories (Feb 9, 1995)
- K915279: Neoprobe Portable Radioscope Detector (Jun 10, 1992)
- K864263: Neoprobe Portable Radioisotope Detector (Dec 29, 1986)

Source page: https://510kreport.com/company/neoprobe