# Electronic Waveform Laboratory, Inc.

- Location (FDA's records): Huntington Beach, CA
- FDA decisions: 6 (1982–2011): 6 510(k) clearances
- Product codes: IPF (2), LWM (1), KZM (1), GZJ (1), NGX (1)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 6 (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
- Compex S.A.: 1 (https://510kreport.com/company/compex)

## Firms that cite its devices most
- Electronic Waveform Lab, Inc.: 2 (https://510kreport.com/company/electronic-waveform-lab)
- Marc Pro: 1 (https://510kreport.com/company/marc-pro)
- Hb Medical, Inc.: 1 (https://510kreport.com/company/hb-medical)

## Its most-cited devices
- K915230: H Wave Muscle Stimulator (1992), cited by 2
- K103738: H-WAVE (2011), cited by 2
- K813601: E.W.L. P-Tens Model (Tens (1982), cited by 1
- K081998: H-Wave Sport (2009), cited by 1

## Recent decisions
- K103738: H-WAVE (Jun 1, 2011)
- K081998: H-Wave Sport (Jul 9, 2009)
- K915230: H Wave Muscle Stimulator (May 8, 1992)
- K873604: E.W.L. P-Tens/H-Wave for General Dentistry (Apr 12, 1988)
- K862121: E.W.L. P-Tens/H-Wave (Jun 17, 1987)
- K813601: E.W.L. P-Tens Model (Tens (Mar 19, 1982)

Source page: https://510kreport.com/company/electronic-waveform-laboratory