SHANGRING

Clamp, Circumcision

WUHU SNNA MEDICAL TREATMENT APPLIANCE TECHNOLOGY C

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

Pre-market Notification Details

• Device ID: K121789
• 510k Number: K121789
• Device Name: SHANGRING
• Classification: Clamp, Circumcision
• Applicant: WUHU SNNA MEDICAL TREATMENT APPLIANCE TECHNOLOGY C 49 PLAIN STREET N. Attleboro, MA 02760
• Contact: Cynthia Nolte
• Correspondent: Cynthia Nolte; WUHU SNNA MEDICAL TREATMENT APPLIANCE TECHNOLOGY C 49 PLAIN STREET N. Attleboro, MA 02760
• Product Code: HFX
• CFR Regulation Number: 884.4530 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2012-06-19
• Decision Date: 2012-08-03
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
26939550822405	K121789	000
26939550822269	K121789	000
26939550822245	K121789	000
26939550822221	K121789	000
26939550822207	K121789	000
26939550822184	K121789	000
26939550822160	K121789	000
26939550822153	K121789	000
26939550822146	K121789	000
26939550822139	K121789	000
26939550822122	K121789	000
26939550822283	K121789	000
26939550822290	K121789	000
26939550822399	K121789	000
26939550822382	K121789	000
26939550822375	K121789	000
26939550822368	K121789	000
26939550822351	K121789	000
26939550822344	K121789	000
26939550822337	K121789	000
26939550822320	K121789	000
26939550822313	K121789	000
26939550822306	K121789	000
26939550822115	K121789	000