MYCOSEL AGAR— 510(k) K832582

Substantially Equivalent

Acuderm, Inc.

FDA 510(k) clearance K832582 for MYCOSEL AGAR, Substantially Equivalent on 1983-09-12. Applicant: Acuderm, Inc..

Clearance details

Applicant: Acuderm, Inc.
Product code: Code JSJ
Advisory panel: Microbiology
Date received: 1983-08-02
Decision date: 1983-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code JSJ

product code JSJ

Malfunction: 520
Total: 520

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.