FILTER SAMPLER BLOOD SERUM FILTER— 510(k) K811036

Substantially Equivalent

Glasrock Plastics, Inc.

FDA 510(k) clearance K811036 for FILTER SAMPLER BLOOD SERUM FILTER, Substantially Equivalent on 1981-04-29. Applicant: Glasrock Plastics, Inc..

Clearance details

Applicant: Glasrock Plastics, Inc.
Product code: Code JKA
Advisory panel: Clinical Chemistry
Date received: 1981-04-16
Decision date: 1981-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code JKA

product code JKA

Injury: 455
Malfunction: 26,686
Other: 4
Total: 27,145

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.