The following data is part of a premarket notification filed by United Pacific Co., Ltd. with the FDA for Kingli Acupuncture Needle.
| Device ID | K990406 |
| 510k Number | K990406 |
| Device Name: | KINGLI ACUPUNCTURE NEEDLE |
| Classification | Needle, Acupuncture, Single Use |
| Applicant | UNITED PACIFIC CO., LTD. 219 SOUTH RAYMOND AVE. Alhambra, CA 91801 |
| Contact | Daniel Ye Hua |
| Correspondent | Daniel Ye Hua UNITED PACIFIC CO., LTD. 219 SOUTH RAYMOND AVE. Alhambra, CA 91801 |
| Product Code | MQX |
| CFR Regulation Number | 880.5580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-02-09 |
| Decision Date | 1999-04-16 |