K254102
- 510(k) number
- K254102
- Device name
- Glucommander
- Applicant
- Glytec, LLC SC · US
- Product code
- NDC — Calculator, Drug Dose
- Decision date
- 2026-05-27
- Date received
- 2025-12-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K254102.pdf
Official FDA record: K254102
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.