# Lifelines, Ltd.

- Location (FDA's records): Crofton, MD
- FDA decisions: 4 (2001–2018): 4 510(k) clearances
- Product codes: OLV (1), GWE (1), GWQ (1), GWL (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 6 (1 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
- Eb Neuro S.P.A.: 1 (https://510kreport.com/company/eb-neuro)
- Carefusion 209, Inc.: 1 (https://510kreport.com/company/carefusion-209)

## Firms that cite its devices most
- Micromed S.P.A.: 1 (https://510kreport.com/company/micromed)
- Eb Neuro S.P.A.: 1 (https://510kreport.com/company/eb-neuro)
- Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek): 1 (https://510kreport.com/company/natus-medical-dba-excel-tech-xltek)
- Wavestate, Inc.: 1 (https://510kreport.com/company/wavestate)
- Nihon Kohden Corporation: 1 (https://510kreport.com/company/nihon-kohden)

## Its most-cited devices
- K101691: Lifelines Photic Stimulator (2010), cited by 3
- K010460: Lifelines Trackit (2001), cited by 2
- K151600: R-40 EEG  Amplifier (2015), cited by 1

## Recent decisions
- K172271: Trackit T4 EEG Amplifier (May 4, 2018)
- K151600: R-40 EEG  Amplifier (Oct 23, 2015)
- K101691: Lifelines Photic Stimulator (Aug 10, 2010)
- K010460: Lifelines Trackit (May 14, 2001)

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