STERI-VERS— 510(k) K810311
Substantially EquivalentThe Hilrad Co.
FDA 510(k) clearance K810311 for STERI-VERS, Substantially Equivalent on 1981-04-17. Applicant: The Hilrad Co.. Device class: 2.
Clearance details
- Applicant
- The Hilrad Co.
- Product code
- Code LDS
- Device class
- Class 2
- Regulation
- 21 CFR 880.6991
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.