GARDNER TYPE BONE MARROW NEEDLE— 510(k) K841301

Substantially Equivalent

Popper & Sons, Inc.

FDA 510(k) clearance K841301 for GARDNER TYPE BONE MARROW NEEDLE, Substantially Equivalent on 1984-06-05. Applicant: Popper & Sons, Inc..

Clearance details

Applicant: Popper & Sons, Inc.
Product code: Code GAA
Advisory panel: General, Plastic Surgery
Date received: 1984-03-30
Decision date: 1984-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code GAA

product code GAA

Malfunction: 834
Total: 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.