Medical Device Manufacturer · KR , Gunpo-Si

The Standard Co., Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - The Standard Co., Ltd. Gastroenterology & Urology ✕
2 devices
1-2 of 2
Cleared Jul 03, 2024
Blue Eye
K241591 · PLL
Gastroenterology & Urology · 30d
Cleared Aug 12, 2022
Blue Eye (TS-905)
K220434 · PLL
Gastroenterology & Urology · 178d
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