The following data is part of a premarket notification filed by Medlogic Global Limited with the FDA for Liquiband Dual, Model Lbd 001.
| Device ID | K102076 |
| 510k Number | K102076 |
| Device Name: | LIQUIBAND DUAL, MODEL LBD 001 |
| Classification | Tissue Adhesive For The Topical Approximation Of Skin |
| Applicant | MEDLOGIC GLOBAL LIMITED WESTERN WOOD WAY LANGAGE SCIENCE PARK Plymouth, Devon, GB Pl7 5bg |
| Contact | Michael Browne |
| Correspondent | Michael Browne MEDLOGIC GLOBAL LIMITED WESTERN WOOD WAY LANGAGE SCIENCE PARK Plymouth, Devon, GB Pl7 5bg |
| Product Code | MPN |
| CFR Regulation Number | 878.4010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-07-26 |
| Decision Date | 2011-02-18 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05036912000932 | K102076 | 000 |
| 05036912000925 | K102076 | 000 |