# Pneupac, Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 20 (1980–2004): 20 510(k) clearances
- Names in FDA's records: Pneupac , Ltd. (19); Pneupac, Inc. (1)
- Product codes: BTL (8), CBK (7), DRM (4), BTI (1)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 7 (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
- Impact Instrumentation, Inc.: 1 (https://510kreport.com/company/impact-instrumentation)

## Firms that cite its devices most
- Airon Corporation: 2 (https://510kreport.com/company/airon)
- Smiths Medical International Ltd., Luton: 2 (https://510kreport.com/company/smiths-medical-international-luton)
- Smiths Medical International, Ltd.: 1 (https://510kreport.com/company/smiths-medical-international)

## Its most-cited devices
- K020899: Parapac 200 Medic, Model P200, & Parapac 200D Medic, Model P200D (2002), cited by 2
- K030803: Parapac 200D Transport, Model V200D (2003), cited by 1
- K960515: Parapac (1996), cited by 1
- K021841: Comppac Ventilator Models 200 & PS11 Power Supply/Charger (2003), cited by 1
- K970158: Babypac (1998), cited by 1
- K862830: Models 2R and 3R Pneupac Ventilator/Resuscitator (1986), cited by 1

## Recent decisions
- K040090: Comppac 200HD; CS12 Power Supply (Aircraft/Vechile); PS11 Power Supply (Mains) (May 27, 2004)
- K030803: Parapac 200D Transport, Model V200D (Sep 29, 2003)
- K021841: Comppac Ventilator Models 200 & PS11 Power Supply/Charger (Jul 17, 2003)
- K020899: Parapac 200 Medic, Model P200, & Parapac 200D Medic, Model P200D (Dec 13, 2002)
- K970158: Babypac (Apr 28, 1998)
- K960515: Parapac (Oct 10, 1996)
- K863410: Patient Valve with Air Entrainment (Jan 12, 1987)
- K862830: Models 2R and 3R Pneupac Ventilator/Resuscitator (Oct 15, 1986)

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