SHANGRING

Clamp, Circumcision

WUHU SNNDA MEDICAL TREATMENT APPLIANCE TECHNOLOGY

The following data is part of a premarket notification filed by Wuhu Snnda Medical Treatment Appliance Technology with the FDA for Shangring.

Pre-market Notification Details

• Device ID: K131373
• 510k Number: K131373
• Device Name: SHANGRING
• Classification: Clamp, Circumcision
• Applicant: WUHU SNNDA MEDICAL TREATMENT APPLIANCE TECHNOLOGY 503 ROOM, 8 BUILDING, 600 LIU ZHOU ROAD Shanghai, CN 200233
• Contact: Bo Gong
• Correspondent: Bo Gong; WUHU SNNDA MEDICAL TREATMENT APPLIANCE TECHNOLOGY 503 ROOM, 8 BUILDING, 600 LIU ZHOU ROAD Shanghai, CN 200233
• Product Code: HFX
• CFR Regulation Number: 884.4530 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2013-05-13
• Decision Date: 2013-06-25