KIDNEY, ARTIFICIAL, C-DAK 1.5— 510(k) K781238
Substantially EquivalentCordis Corp.
FDA 510(k) clearance K781238 for KIDNEY, ARTIFICIAL, C-DAK 1.5, Substantially Equivalent on 1978-08-31. Applicant: Cordis Corp.. Device class: 2.
Clearance details
- Applicant
- Cordis Corp.
- Product code
- Code DJC
- Device class
- Class 2
- Regulation
- 21 CFR 862.3610
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.