The following data is part of a premarket notification filed by Bard Peripheral Vascular, Inc with the FDA for Liverty™ Tips Access Set.
| Device ID | K221440 |
| 510k Number | K221440 |
| Device Name: | Liverty™ TIPS Access Set |
| Classification | Introducer, Catheter |
| Applicant | Bard Peripheral Vascular, Inc 1625 West 3rd Street Tempe, AZ 85281 |
| Contact | Scott Johnson |
| Correspondent | Prithul Bom REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2022-05-17 |
| Decision Date | 2022-05-31 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00382903064663 | K221440 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LIVERTY 90469326 not registered Live/Pending |
C. R. BARD, INC. 2021-01-15 |
![]() LIVERTY 85780089 4511776 Live/Registered |
GOLDEN BIOTECHNOLOGY CORPORATION 2012-11-15 |