PORTEX TRACHEAL TUBE, SIZES 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5— 510(k) K083119

Substantially Equivalent

Smiths Medical Asd, Inc.

FDA 510(k) clearance K083119 for PORTEX TRACHEAL TUBE, SIZES 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, Substantially Equivalent on 2009-06-26. Applicant: Smiths Medical Asd, Inc.. Device class: 2.

Clearance details

Applicant
Smiths Medical Asd, Inc.
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
Abbreviated
Location
Hythe, Kent, GB
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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 →

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