SYMBIOSIS BONE MARROW BIOPSY NEEDLE— 510(k) K925416

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K925416 for SYMBIOSIS BONE MARROW BIOPSY NEEDLE, Substantially Equivalent on 1993-02-23. Applicant: Symbiosis Corp..

Clearance details

Applicant: Symbiosis Corp.
Product code: Code GAA
Advisory panel: General, Plastic Surgery
Date received: 1992-10-27
Decision date: 1993-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, 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.