MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM— 510(k) K971105

Name: FDA 510(k) clearance K971105
Creator: U.S. Food and Drug Administration
Published: 1997-07-11

Substantially Equivalent

Avecor Cardiovascular, Inc.

FDA 510(k) clearance K971105 for MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM, Substantially Equivalent on 1997-07-11. Applicant: Avecor Cardiovascular, Inc.. Device class: 2.

Clearance details

Applicant: Avecor Cardiovascular, Inc.
Product code: Code DTN
Device class: Class 2
Regulation: 21 CFR 870.4400
Advisory panel: Cardiovascular
Date received: 1997-03-26
Decision date: 1997-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DTN

product code DTN

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.