FlexCath Advance Steerable Sheath and Dilator— 510(k) K202620

Substantially Equivalent

Medtronic Cryocath, LP

FDA 510(k) clearance K202620 for FlexCath Advance Steerable Sheath and Dilator, Substantially Equivalent on 2020-11-13. Applicant: Medtronic Cryocath, LP. Device class: 2.

Clearance details

Applicant
Medtronic Cryocath, LP
Product code
Code DRA
Device class
Class 2
Regulation
21 CFR 870.1280
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Minneapolis, MN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DRA

product code DRA
Death
156
Injury
3,133
Malfunction
6,266
Total
9,555

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.