The following data is part of a premarket notification filed by Advanced Medical Solutions Limited with the FDA for Liquiband Xl.
| Device ID | K211878 |
| 510k Number | K211878 |
| Device Name: | LiquiBand XL |
| Classification | Cutaneous Tissue Adhesive With Mesh |
| Applicant | Advanced Medical Solutions Limited Western Wood Way , Langage Science Park Plymouth, GB PL7 5BG |
| Contact | Martin Mitchell |
| Correspondent | Martin Mitchell Advanced Medical Solutions Limited Western Wood Way , Langage Science Park Plymouth, GB PL7 5BG |
| Product Code | OMD |
| CFR Regulation Number | 878.4011 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-06-21 |
| Decision Date | 2022-05-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05036912001489 | K211878 | 000 |
| 05036912001397 | K211878 | 000 |
| 05036912001243 | K211878 | 000 |
| 05036912001663 | K211878 | 000 |
| 05036912001571 | K211878 | 000 |
| 05036912001540 | K211878 | 000 |
| 05036912001519 | K211878 | 000 |
| 40612479267921 | K211878 | 000 |
| 20197344009401 | K211878 | 000 |