MEDICAL OSCILLOSCOPE MEMORY SCOPE— 510(k) K760721

Name: FDA 510(k) clearance K760721
Creator: U.S. Food and Drug Administration
Published: 1976-10-06

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K760721 for MEDICAL OSCILLOSCOPE MEMORY SCOPE, Substantially Equivalent on 1976-10-06. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code DXJ
Device class: Class 2
Regulation: 21 CFR 870.2450
Advisory panel: Cardiovascular
Date received: 1976-09-27
Decision date: 1976-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DXJ

view all

K212003 — ESSENZ Patient Monitor2021-11-10
K212208 — Philips IntelliVue GuardianSoftware (Rev. E.0X)2021-09-30
K201162 — Essence 55SP Large Monitor System2020-08-27
K173107 — Vios Central Station Monitor Software, Vios Central Server Software2018-07-26
K180534 — Philips IntelliVue GuardianSoftware2018-07-16

More clearances from Abbott Laboratories

view all

K252424 — Anti-HCV Next2026-04-28
K243500 — ARCHITECT iGentamicin2025-07-09
K243168 — Alinity i Rubella IgG2025-06-20
K243283 — Alinity h-series System2025-02-20
K233932 — Alinity i Toxo IgM2024-08-30

Adverse events under product code DXJ

product code DXJ

Death: 2
Total: 2

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.