The following data is part of a premarket notification filed by Numed, Inc. with the FDA for Mini Ghost Pta Catheter, Model 507.
Device ID | K051343 |
510k Number | K051343 |
Device Name: | MINI GHOST PTA CATHETER, MODEL 507 |
Classification | Catheter, Percutaneous |
Applicant | NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
Contact | Nichelle Laflesh |
Correspondent | Nichelle Laflesh NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
Product Code | DQY |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-05-23 |
Decision Date | 2005-07-28 |
Summary: | summary |