# Howtek, Inc.

- Location (FDA's records): Hudson, NH
- FDA decisions: 5 (1996–2002): 5 510(k) clearances
- Product codes: LMA (3), LMD (1), LLZ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Star Technologies, Inc.: 1 (https://510kreport.com/company/star-technologies)
- Applicare Medical Imaging, B.V.: 1 (https://510kreport.com/company/applicare-medical-imaging)

## Firms that cite its devices most
- Lumisys, Inc.: 1 (https://510kreport.com/company/lumisys)
- Microtek International, Inc.: 1 (https://510kreport.com/company/microtek-international)

## Its most-cited devices
- K972191: Digitizer Director (HSC025-01) (1997), cited by 1
- K021949: Fulcrum (2002), cited by 1

## Recent decisions
- K021949: Fulcrum (Aug 12, 2002)
- K973081: Digitizer Director: Image Compression Module (HO4059-Rev 2.0) (Nov 5, 1997)
- K972191: Digitizer Director (HSC025-01) (Sep 8, 1997)
- K970908: Howtek 960 (May 20, 1997)
- K953117: Scanmaster DX (Jan 18, 1996)

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