The following data is part of a premarket notification filed by Advanced Medical Products, Inc. with the FDA for Arachnophlebectomy Needle.
| Device ID | K000932 |
| 510k Number | K000932 |
| Device Name: | ARACHNOPHLEBECTOMY NEEDLE |
| Classification | Stylet, Surgical, General & Plastic Surgery |
| Applicant | ADVANCED MEDICAL PRODUCTS, INC. 11902 SIMPSON RD. Clarksville, MD 21029 |
| Contact | Charles H Kyper |
| Correspondent | Charles H Kyper ADVANCED MEDICAL PRODUCTS, INC. 11902 SIMPSON RD. Clarksville, MD 21029 |
| Product Code | GAH |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-03-23 |
| Decision Date | 2000-05-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ARACHNOPHLEBECTOMY NEEDLE 76153424 not registered Dead/Abandoned |
Advanced Medical Products, Inc. 2000-10-24 |