Optimos™ Cystotome— 510(k) K223256

Substantially Equivalent

Taewoong Medical Co., Ltd.

FDA 510(k) clearance K223256 for Optimos™ Cystotome, Substantially Equivalent on 2023-04-05. Applicant: Taewoong Medical Co., Ltd..

Clearance details

Applicant
Taewoong Medical Co., Ltd.
Product code
Code KNS
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Gimpo-Si, KR
Download summary PDFView on FDA.gov ↗

Adverse events under product code KNS

product code KNS
Death
44
Injury
2,361
Malfunction
4,771
Total
7,176

Source: openFDA MAUDE database, through . 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.