Pivot System Sterilization case— 510(k) K181845
Substantially EquivalentRp Medical, Inc.
FDA 510(k) clearance K181845 for Pivot System Sterilization case, Substantially Equivalent on 2019-11-25. Applicant: Rp Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Rp Medical, Inc.
- Product code
- Code KCT
- Device class
- Class 2
- Regulation
- 21 CFR 880.6850
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Maple Ridge, CA
Recent devices under product code KCT
view allData sourced from openFDA. This site is unofficial and independent of the FDA.