# Fasstech

- Location (FDA's records): Burlington, MA
- FDA decisions: 9 (1993–2007): 9 510(k) clearances
- Product codes: HCC (5), IKN (3), KQX (1)
- Predicates its devices cite: 9 (5 its own); citations of its devices by later devices: 7 (5 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
- Davicon, Inc.: 2 (https://510kreport.com/company/davicon)
- Futrex, Inc.: 1 (https://510kreport.com/company/futrex)
- J-Tech Medical, Inc.: 1 (https://510kreport.com/company/j-tech-medical)

## Firms that cite its devices most
- Dorsa VI Pty., Ltd.: 1 (https://510kreport.com/company/dorsa-vi)
- Precision Biometrics, Inc.: 1 (https://510kreport.com/company/precision-biometrics)

## Its most-cited devices
- K023209: Insight Millennium Iii (2003), cited by 3
- K990778: Insight Millennium (1999), cited by 2
- K063447: Insight Discovery (2007), cited by 1
- K011964: Insight Millennium Plus (2001), cited by 1

## Recent decisions
- K063447: Insight Discovery (Aug 16, 2007)
- K033452: CWAS 1000 (Nov 28, 2003)
- K023209: Insight Millennium Iii (Oct 10, 2003)
- K011964: Insight Millennium Plus (Sep 20, 2001)
- K011983: Insight Genesis (Aug 30, 2001)
- K990778: Insight Millennium (Jun 3, 1999)
- K961212: Spinal Touch (Jun 12, 1996)
- K940050: Focus Emg (Feb 24, 1995)

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