BIVONA WIRE REINFORCED PEDIATRIC TRACHEOSTOMY TUBE— 510(k) K912469

Substantially Equivalent

Bivona Medical Technologies

FDA 510(k) clearance K912469 for BIVONA WIRE REINFORCED PEDIATRIC TRACHEOSTOMY TUBE, Substantially Equivalent on 1991-06-19. Applicant: Bivona Medical Technologies. Device class: 2.

Clearance details

Applicant
Bivona Medical Technologies
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
Gary, IN, 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 →

Recalls naming K912469

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 K912469.

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