KANGSHENG BRAND/KANGNIAN BRAND/UNILINK BRAND/HUAZHONG BRAND ACUPUNCTURE NEEDLES

Needle, Acupuncture, Single Use

DAXIN LI

The following data is part of a premarket notification filed by Daxin Li with the FDA for Kangsheng Brand/kangnian Brand/unilink Brand/huazhong Brand Acupuncture Needles.

Pre-market Notification Details

• Device ID: K052731
• 510k Number: K052731
• Device Name: KANGSHENG BRAND/KANGNIAN BRAND/UNILINK BRAND/HUAZHONG BRAND ACUPUNCTURE NEEDLES
• Classification: Needle, Acupuncture, Single Use
• Applicant: DAXIN LI 2600 MISSION STREET, SUITE 100 San Marino, CA 91108
• Contact: Yingchao Xiao
• Correspondent: Yingchao Xiao; DAXIN LI 2600 MISSION STREET, SUITE 100 San Marino, CA 91108
• Product Code: MQX
• CFR Regulation Number: 880.5580 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2005-09-29
• Decision Date: 2006-02-01
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
09351885000236	K052731	000
09351885000106	K052731	000
09351885000083	K052731	000
09351885000076	K052731	000
09351885000069	K052731	000
09351885000052	K052731	000
09351885000045	K052731	000
09351885000038	K052731	000
09351885000021	K052731	000
09351885000014	K052731	000
09351885000113	K052731	000
09351885000120	K052731	000
09351885000137	K052731	000
09351885000229	K052731	000
09351885000212	K052731	000
09351885000205	K052731	000
09351885000199	K052731	000
09351885000182	K052731	000
09351885000175	K052731	000
09351885000168	K052731	000
09351885000151	K052731	000
09351885000144	K052731	000
09351885000007	K052731	000