SYMBIOSIS ENT SURGICAL INSTRUMENTS— 510(k) K931793

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K931793 for SYMBIOSIS ENT SURGICAL INSTRUMENTS, Substantially Equivalent on 1993-07-22. Applicant: Symbiosis Corp..

Clearance details

Applicant: Symbiosis Corp.
Product code: Code LRC
Advisory panel: Ear, Nose, Throat
Date received: 1993-04-12
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LRC

product code LRC

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.