STERIS SYSTEM 1 PROCESSOR AND 20 STERILANT— 510(k) K875280
Substantially EquivalentSteris C/O Medical Device Consultants, Inc.
FDA 510(k) clearance K875280 for STERIS SYSTEM 1 PROCESSOR AND 20 STERILANT, Substantially Equivalent on 1988-09-13. Applicant: Steris C/O Medical Device Consultants, Inc.. Device class: 2.
Clearance details
- Applicant
- Steris C/O Medical Device Consultants, Inc.
- Product code
- Code MED
- Device class
- Class 2
- Regulation
- 21 CFR 880.6885
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Attleboro, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.