# Camntech, Ltd.

- Location (FDA's records): Papworth Everard, Cambridgeshire, GB
- FDA decisions: 2 (2010–2014): 2 510(k) clearances
- Product codes: LEL (1), MWJ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 4 (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 whose devices it cites most
- Mini-Mitter Co., Inc.: 2 (https://510kreport.com/company/mini-mitter)
- General Electric Medical Systems Information Techn: 1 (https://510kreport.com/company/general-electric-medical-systems-information-techn)

## Firms that cite its devices most
- Healthwatch, Ltd.: 1 (https://510kreport.com/company/healthwatch)
- Mc10, Inc.: 1 (https://510kreport.com/company/mc10)
- Arbor Medical Innovations, LLC: 1 (https://510kreport.com/company/arbor-medical-innovations)
- Condor Instruments Ltda. - Epp: 1 (https://510kreport.com/company/condor-instruments-ltda-epp)

## Its most-cited devices
- K132764: Motion Watch and Pro-Diary (2014), cited by 4

## Recent decisions
- K132764: Motion Watch and Pro-Diary (Jan 21, 2014)
- K100266: Actiwave 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, Actiwave Cardio Model 08-514, 08-521, 08-536, 08-557, 08-603 (Apr 29, 2010)

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