# Gibeck Respiration

- Location (FDA's records): Schaumburg, IL
- FDA decisions: 6 (1987–1988): 6 510(k) clearances
- Product codes: BYD (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Munktell Filter AB: 1 (https://510kreport.com/company/munktell-filter)

## Its most-cited devices
- K881657: Humid-Vent Filter (1988), cited by 1

## Recent decisions
- K881657: Humid-Vent Filter (Jun 24, 1988)
- K881656: Humid-Vent 2 S Flex (Jun 16, 1988)
- K881644: Humid-Vent 2 S (Jun 10, 1988)
- K873768: Humid-Vent (R) 2 Port (Nov 24, 1987)
- K873767: Humid-Vent (R) Mini (Nov 6, 1987)
- K872153: Stom-Vent (Aug 3, 1987)

Source page: https://510kreport.com/company/gibeck-respiration