K223835
- 510(k) number
- K223835
- Device name
- MA-40, MA-112
- Applicant
- Medify Air, LLC FL · US
- Product code
- FRF — Cleaner, Air, Medical Recirculating
- Decision date
- 2023-09-18
- Date received
- 2022-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K223835
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.