VISION HOLLOW FIBER OXYGENATOR WITH GUARDIAN COATING— 510(k) K023381

Substantially Equivalent

Gish Biomedical, Inc.

FDA 510(k) clearance K023381 for VISION HOLLOW FIBER OXYGENATOR WITH GUARDIAN COATING, Substantially Equivalent on 2003-03-31. Applicant: Gish Biomedical, Inc.. Device class: 2.

Clearance details

Applicant
Gish Biomedical, Inc.
Product code
Code DTZ
Device class
Class 2
Regulation
21 CFR 870.4350
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Houston, TX, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DTZ

product code DTZ
Death
182
Injury
422
Malfunction
3,636
Total
4,240

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.