FDA applicant
Respiratory Support Products, Inc.
FDA records 27 decisions for Respiratory Support Products, Inc. (Costa Mesa, CA) from 1979 to 1999: 27 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 8 recalls are linked to its devices, 6 Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Respiratory Support Products, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Respiratory Support Products, Inc. since 2007.
Recalls per year
1in 2025
Class I Class II/III not classified
Planning a device like Respiratory Support Products, Inc.’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 “Respiratory”
FDA records each applicant name separately; these may or may not be the same firm.