HYBRITECH DATA STATION— 510(k) K834300

Name: FDA 510(k) clearance K834300
Creator: U.S. Food and Drug Administration
Published: 1984-02-21

Substantially Equivalent

Hybritech, Inc.

FDA 510(k) clearance K834300 for HYBRITECH DATA STATION, Substantially Equivalent on 1984-02-21. Applicant: Hybritech, Inc.. Device class: 1.

Clearance details

Applicant: Hybritech, Inc.
Product code: Code JQP
Device class: Class 1
Regulation: 21 CFR 862.2100
Advisory panel: Clinical Chemistry
Date received: 1983-12-09
Decision date: 1984-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JQP

product code JQP

Death: 3
Malfunction: 690
Total: 693

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.