MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS— 510(k) K885175

Substantially Equivalent

Possis Medical, Inc.

FDA 510(k) clearance K885175 for MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS, Substantially Equivalent on 1989-07-14. Applicant: Possis Medical, Inc..

Clearance details

Applicant: Possis Medical, Inc.
Product code: Code DTB
Advisory panel: Cardiovascular
Date received: 1988-12-14
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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Adverse events under product code DTB

product code DTB

Death: 1,491
Injury: 67,311
Malfunction: 79,368
Other: 10
Total: 148,180

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.