AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129)— 510(k) K030340

Substantially Equivalent

Cytomedix

FDA 510(k) clearance K030340 for AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129), Substantially Equivalent on 2003-04-11. Applicant: Cytomedix.

Clearance details

Applicant: Cytomedix
Product code: Code JQC
Advisory panel: Clinical Chemistry
Date received: 2003-01-31
Decision date: 2003-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JQC

product code JQC

Other: 1
Total: 1

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.