K233553
- 510(k) number
- K233553
- Device name
- MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI Adapter
- Applicant
- Thayer Medical Corporation AZ · US
- Product code
- CAF — Nebulizer (Direct Patient Interface)
- Decision date
- 2024-06-18
- Date received
- 2023-11-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Anesthesiology
510(k) Summary (official FDA PDF): K233553.pdf
Official FDA record: K233553
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.