The following data is part of a premarket notification filed by Atrium Medical Corp. with the FDA for Modification To Atrium Medical Corporation Clearway Ptfe Balloon Catheter.
| Device ID | K020634 |
| 510k Number | K020634 |
| Device Name: | MODIFICATION TO ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER |
| Classification | Catheter, Embolectomy |
| Applicant | ATRIUM MEDICAL CORP. 5 WENTWORTH DR. Hudson, NH 03051 |
| Contact | Joseph P De Paola |
| Correspondent | Joseph P De Paola ATRIUM MEDICAL CORP. 5 WENTWORTH DR. Hudson, NH 03051 |
| Product Code | DXE |
| CFR Regulation Number | 870.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-02-27 |
| Decision Date | 2002-05-08 |