# Aerotel, Ltd.

- Location (FDA's records): Israel, IL
- FDA decisions: 6 (1994–1998): 6 510(k) clearances
- Product codes: DXH (5), DPS (1)
- Predicates its devices cite: 5 (4 its own); citations of its devices by later devices: 9 (4 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
- Meridian Medical Technologies, Inc.: 1 (https://510kreport.com/company/meridian-medical-technologies)

## Firms that cite its devices most
- Aerotel Medical Systems (1998), Ltd.: 4 (https://510kreport.com/company/aerotel-medical-systems-1998)
- Meridian Medical Technologies, Inc.: 1 (https://510kreport.com/company/meridian-medical-technologies)

## Its most-cited devices
- K930314: Heartline Transtelephonic Ecg Receiving Console (1994), cited by 3
- K931020: HEART 1001 (1995), cited by 3
- K950004: Heartview (TM) 12-Lead Electrocardiograph Recorder/Transmitter (1995), cited by 3

## Recent decisions
- K980144: Heartview P12/8 Electrocardiograph Recorder and Transmitter (Jun 16, 1998)
- K953762: Heart 400 Ecg Transmitter (Jul 18, 1996)
- K961362: Aerotel Telelink Ecg Telephonic Receiving Interface (Jul 10, 1996)
- K950004: Heartview (TM) 12-Lead Electrocardiograph Recorder/Transmitter (Oct 24, 1995)
- K931020: HEART 1001 (Jan 11, 1995)
- K930314: Heartline Transtelephonic Ecg Receiving Console (Mar 18, 1994)

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