CORDIS CSF RESERVOIR— 510(k) K950315
UnknownCordis Corp.
FDA 510(k) clearance K950315 for CORDIS CSF RESERVOIR, Unknown on 1995-05-09. Applicant: Cordis Corp.. Device class: 2.
Clearance details
- Applicant
- Cordis Corp.
- Product code
- Code LKG
- Device class
- Class 2
- Regulation
- 21 CFR 882.5550
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Miami, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.