Data / Medical devices / Ventilator, External Body, Negative Pressure, Adult (Cuirass)
Ventilator, External Body, Negative Pressure, Adult (Cuirass) (BYT): 3 FDA-registered makers in 3 countries
3 establishments in 3 countries are registered with the FDA to make Ventilator, External Body, Negative Pressure, Adult (Cuirass) (product code BYT, Class 2, 21 CFR 868.5935). 3 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 21 510(k) clearances under this code, the latest on October 8, 2008, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- BYT
- Device class
- 2
- Regulation
- 868.5935
- Medical specialty
- Anesthesiology
- Life sustaining or supporting
- Yes
Makers by country
| Country | Makers |
|---|---|
| Italy | 1 |
| United States | 1 |
| United Kingdom | 1 |
Makers of Ventilator, External Body, Negative Pressure, Adult (Cuirass)
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dima Italia SRL | Bologna, Italy | Manufacturer | 1 | May 29, 2008 | 0 | 0 | 0 | api.fda.gov |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Specification developer | 1 | December 22, 1989 | 0 | 0 | 0 | api.fda.gov |
| United Hayek Industries Manufacturing Ltd | London Barnet, United Kingdom | Manufacturer | 1 | October 8, 2008 | 0 | 0 | 0 | api.fda.gov |
Updated October 8, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.