RAIN Sheath Transradial— 510(k) K181592
Substantially EquivalentCordis Corporation
FDA 510(k) clearance K181592 for RAIN Sheath Transradial, Substantially Equivalent on 2018-08-15. Applicant: Cordis Corporation. Device class: 2.
Clearance details
- Applicant
- Cordis Corporation
- Product code
- Code DYB
- Device class
- Class 2
- Regulation
- 21 CFR 870.1340
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Milpitas, CA, US
Recent devices under product code DYB
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- K201377 — SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
Adverse events under product code DYB
product code DYB- Death
- 808
- Injury
- 5,922
- Malfunction
- 16,516
- Other
- 5
- Total
- 23,251
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.