# Immunoprobe, Inc.

- Location (FDA's records): Washington, D.C., DC
- FDA decisions: 14 (1994–1997): 14 510(k) clearances
- Product codes: MID (5), JNL (4), MOB (2), LJZ (1), GOD (1), LLM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bio-Rad Laboratories, Inc.: 1 (https://510kreport.com/company/bio-rad-laboratories)

## Its most-cited devices
- K951549: Ebna Igg Eia Test System (1996), cited by 1

## Recent decisions
- K972406: Adenovirus Antigen Detection Elisa Test System (Dec 22, 1997)
- K971393: Mycoplasma Igg Elisa Test System (Jul 14, 1997)
- K961764: PR-3 Elisa Test System (Aug 19, 1996)
- K961765: Mpo Elisa Test System (Aug 19, 1996)
- K951549: Ebna Igg Eia Test System (Apr 29, 1996)
- K952521: Cardiolipin Igm Eia Test System (Feb 9, 1996)
- K952523: Cardiolipin Igg Eia Test Kit (Feb 9, 1996)
- K952522: Cardiolipin Iga Eia Test System (Feb 9, 1996)

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