KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS— 510(k) K113333

Substantially Equivalent

Kimberly-Clark Corporation

FDA 510(k) clearance K113333 for KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS, Substantially Equivalent on 2012-05-11. Applicant: Kimberly-Clark Corporation. Device class: 2.

Clearance details

Applicant
Kimberly-Clark Corporation
Product code
Code BTR
Device class
Class 2
Regulation
21 CFR 868.5730
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Roswell, GA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code BTR

product code BTR
Death
92
Injury
1,263
Malfunction
7,475
Other
2
Total
8,832

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.