# Cottrell, Ltd.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 9 (1990–1999): 9 510(k) clearances
- Product codes: MED (3), LRJ (1), MMN (1), JOJ (1), EFS (1), MMP (1), KCT (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 4 (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
- Johnson & Johnson Medical, Inc.: 3 (https://510kreport.com/company/johnson-johnson-medical)
- Steris C/O Medical Device Consultants, Inc.: 1 (https://510kreport.com/company/steris-c-o-medical-device-consultants)

## Firms that cite its devices most
- Filmtech, Inc.: 1 (https://510kreport.com/company/filmtech)
- Pinnacle Products, Inc.: 1 (https://510kreport.com/company/pinnacle-products)
- Sterilox Technologies, Inc.: 1 (https://510kreport.com/company/sterilox-technologies)

## Its most-cited devices
- K972708: Endo-Spor Plus / Hyprocide (1999), cited by 1
- K952234: Barrier All Film (1995), cited by 1
- K932922: Procide 14 N.S., Omnicide/Liquid & Plus Liq Activator (1995), cited by 1
- K952241: Protouch Overglove (1995), cited by 1

## Recent decisions
- K972708: Endo-Spor Plus / Hyprocide (Sep 13, 1999)
- K970726: Vapocide (May 18, 1998)
- K960089: Prochek G Glutaraldehyde Concentration Level Indicator (Apr 4, 1996)
- K952241: Protouch Overglove (Aug 7, 1995)
- K952234: Barrier All Film (Jul 31, 1995)
- K932922: Procide 14 N.S., Omnicide/Liquid & Plus Liq Activator (Jul 3, 1995)
- K951983: Imni-II (Jun 20, 1995)
- K945575: Pro Barrier (TM) Tube Sox (TM) (Mar 6, 1995)

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