E-RAM— 510(k) K884126

Name: FDA 510(k) clearance K884126
Creator: U.S. Food and Drug Administration
Published: 1989-10-30

Substantially Equivalent

Reynolds Medical , Ltd.

FDA 510(k) clearance K884126 for E-RAM, Substantially Equivalent on 1989-10-30. Applicant: Reynolds Medical , Ltd.. Device class: 2.

Clearance details

Applicant: Reynolds Medical , Ltd.
Product code: Code DSH
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 1988-09-30
Decision date: 1989-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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K011837 — LIFECARD CF 7 DAY2001-07-13
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Adverse events under product code DSH

product code DSH

Death: 3
Injury: 652
Total: 655

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.