GEN. DIAG. CHROMOSTRATE REF. PLASMA— 510(k) K850409

Substantially Equivalent

Warner-Lambert Co.

FDA 510(k) clearance K850409 for GEN. DIAG. CHROMOSTRATE REF. PLASMA, Substantially Equivalent on 1985-05-08. Applicant: Warner-Lambert Co..

Clearance details

Applicant: Warner-Lambert Co.
Product code: Code JPA
Advisory panel: Hematology
Date received: 1985-02-04
Decision date: 1985-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Morris Plains, NJ, US

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Adverse events under product code JPA

product code JPA

Death: 6
Total: 6

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.