CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC...— 510(k) K111117

Unknown

Teleflexmedical, Inc.

FDA 510(k) clearance K111117 for CANNON II PLUS CHRONIC HEMODIALYSIS CATHETER, EDGE CHRONIC HEMODIALYSIS CATHETER, NEXTSTEP(R) RETROGRADE CHRONIC..., Unknown on 2011-06-30. Applicant: Teleflexmedical, Inc.. Device class: 2.

Clearance details

Applicant
Teleflexmedical, Inc.
Product code
Code MSD
Device class
Class 2
Regulation
21 CFR 876.5540
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Unknown
Clearance type
Special
Location
Reading, PA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code MSD

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More clearances from Teleflexmedical, Inc.

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Adverse events under product code MSD

product code MSD
Death
67
Injury
545
Malfunction
3,661
Total
4,273

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 →

Recalls naming K111117

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K111117.

Data sourced from openFDA. This site is unofficial and independent of the FDA.