TOXO-CUBE— 510(k) K903968

Substantially Equivalent

Difco Laboratories, Inc.

FDA 510(k) clearance K903968 for TOXO-CUBE, Substantially Equivalent on 1990-12-18. Applicant: Difco Laboratories, Inc..

Clearance details

Applicant: Difco Laboratories, Inc.
Product code: Code LGD
Advisory panel: Microbiology
Date received: 1990-08-28
Decision date: 1990-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ann Arbor, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LGD

product code LGD

Malfunction: 502
Total: 502

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.