K231895
- 510(k) number
- K231895
- Device name
- Maxtec MaxBlend2+p
- Applicant
- Maxtec, LLC UT · US
- Product code
- BZR — Mixer, Breathing Gases, Anesthesia Inhalation
- Decision date
- 2023-12-04
- Date received
- 2023-06-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K231895.pdf
Official FDA record: K231895
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.