SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND— 510(k) K932265

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K932265 for SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND, Substantially Equivalent on 1993-08-09. Applicant: Symbiosis Corp..

Clearance details

Applicant: Symbiosis Corp.
Product code: Code FCL
Advisory panel: Gastroenterology, Urology
Date received: 1993-04-20
Decision date: 1993-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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Adverse events under product code FCL

product code FCL

Death: 5
Total: 5

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.