Q-SCAN II AND Q-SCAN III— 510(k) K864149

Name: FDA 510(k) clearance K864149
Creator: U.S. Food and Drug Administration
Published: 1986-12-10

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K864149 for Q-SCAN II AND Q-SCAN III, Substantially Equivalent on 1986-12-10. Applicant: Quinton, Inc.. Device class: 2.

Clearance details

Applicant: Quinton, Inc.
Product code: Code DSI
Device class: Class 2
Regulation: 21 CFR 870.1025
Advisory panel: Cardiovascular
Date received: 1986-10-22
Decision date: 1986-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Quinton, Inc.

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K032038 — PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 926012003-09-05
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K003576 — Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 0005032001-01-25
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Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

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.