CORDIS TUNNELER— 510(k) K932273
Substantially EquivalentCordis Corp.
FDA 510(k) clearance K932273 for CORDIS TUNNELER, Substantially Equivalent on 1993-08-23. Applicant: Cordis Corp.. Device class: 1.
Clearance details
- Applicant
- Cordis Corp.
- Product code
- Code GYK
- Device class
- Class 1
- Regulation
- 21 CFR 882.4545
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.