ARRW EVOLUTION— 510(k) K112896

Substantially Equivalent

Arrow International (Subsidiary of Teleflex Inc.)

FDA 510(k) clearance K112896 for ARRW EVOLUTION, Substantially Equivalent on 2012-05-10. Applicant: Arrow International (Subsidiary of Teleflex Inc.). Device class: 2.

Clearance details

Applicant
Arrow International (Subsidiary of Teleflex Inc.)
Product code
Code LJS
Device class
Class 2
Regulation
21 CFR 880.5970
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Reading, PA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LJS

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More clearances from Arrow International (Subsidiary of Teleflex Inc.)

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Adverse events under product code LJS

product code LJS
Death
31
Injury
2,791
Malfunction
18,374
Other
5
Total
21,201

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 K112896

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 K112896.

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