CS 9600— 510(k) K200183
Substantially EquivalentTrophy
FDA 510(k) clearance K200183 for CS 9600, Substantially Equivalent on 2020-03-13. Applicant: Trophy. Device class: 2.
Clearance details
- Applicant
- Trophy
- Product code
- Code OAS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1750
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Croissy-Beaubourg, FR
Recent devices under product code OAS
view allMore clearances from Trophy
view allRecalls naming K200183
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K200183.
Data sourced from openFDA. This site is unofficial and independent of the FDA.