FDA applicant
Respironics Respiratory Drug Delivery (Uk), Ltd.
FDA records 2 decisions for Respironics Respiratory Drug Delivery (Uk), Ltd. (Chichester, GB) from 2011 to 2017: 2 510(k) clearances. All are in product code CAF (Nebulizer (Direct Patient Interface)). Its devices cite 6 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Respironics Respiratory Drug Delivery (Uk), Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2011.
Planning a device like Respironics Respiratory Drug Delivery…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Respironics”
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