K260766
- 510(k) number
- K260766
- Device name
- Celerity 5 HP Biological Indicator (LCB052)
- Applicant
- STERIS Corporation OH · US
- Product code
- FRC — Indicator, Biological Sterilization Process
- Decision date
- 2026-04-08
- Date received
- 2026-03-09
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K260766.pdf
Official FDA record: K260766
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.