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 |