LARYNGECTOMY TUBE, CUFFED— 510(k) K860176

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K860176 for LARYNGECTOMY TUBE, CUFFED, Substantially Equivalent on 1986-01-27. Applicant: Sheridan Catheter Corp.. Device class: 2.

Clearance details

Applicant
Sheridan Catheter Corp.
Product code
Code BTO
Device class
Class 2
Regulation
21 CFR 868.5800
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Argyle, NY, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code BTO

product code BTO
Death
14
Injury
328
Malfunction
1,851
Total
2,193

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.