MODIFICATION OF: CELL-DYN 1200 SYSTEM— 510(k) K992444

Name: FDA 510(k) clearance K992444
Creator: U.S. Food and Drug Administration
Published: 1999-09-24

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K992444 for MODIFICATION OF: CELL-DYN 1200 SYSTEM, Substantially Equivalent on 1999-09-24. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant: Abbott Laboratories
Product code: Code GKZ
Device class: Class 2
Regulation: 21 CFR 864.5220
Advisory panel: Hematology
Date received: 1999-07-22
Decision date: 1999-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GKZ

product code GKZ

Malfunction: 1,205
Total: 1,205

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.