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.
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 |
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 |