# Myelotec, Inc.

- Location (FDA's records): Mt. Airy, MD
- FDA decisions: 3 (1996–2013): 3 510(k) clearances
- Names in FDA's records: Myelotec, Inc. (2); Myelotec (1)
- Product codes: HRX (3)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Henke Sass Wolf of America, Inc.: 1 (https://510kreport.com/company/henke-sass-wolf-of-america)
- Medic Evaluation Devices & Instruments Corp.: 1 (https://510kreport.com/company/medic-evaluation-devices-instruments)
- Sofamor Danek Mfg., Inc.: 1 (https://510kreport.com/company/sofamor-danek-mfg)

## Firms that cite its devices most
- Imedicom Co., Ltd.: 2 (https://510kreport.com/company/imedicom)
- Advanced Medical Systems Group Srl: 1 (https://510kreport.com/company/advanced-medical-systems-group)

## Its most-cited devices
- K980734: Myelotec Video Guided Catheter (1998), cited by 3

## Recent decisions
- K122411: J-Scope System (Feb 11, 2013)
- K980734: Myelotec Video Guided Catheter (Aug 11, 1998)
- K960194: Myelotec Myeloscope (Sep 4, 1996)

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