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 |