K251666
- 510(k) number
- K251666
- Device name
- SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900
- Applicant
- STERIS Corporation OH · US
- Product code
- MED — Sterilant, Medical Devices
- Decision date
- 2026-04-08
- Date received
- 2025-05-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K251666.pdf
Official FDA record: K251666
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.