DIAMOND'S MEDIUM MODIFIED— 510(k) K881995

Substantially Equivalent

Remel Co.

FDA 510(k) clearance K881995 for DIAMOND'S MEDIUM MODIFIED, Substantially Equivalent on 1988-06-02. Applicant: Remel Co..

Clearance details

Applicant: Remel Co.
Product code: Code KZI
Advisory panel: Microbiology
Date received: 1988-05-12
Decision date: 1988-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

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Adverse events under product code KZI

product code KZI

Malfunction: 2,834
Total: 2,834

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.