The following data is part of a premarket notification filed by Medlogic Global Limited with the FDA for Liquishield Liquid Bandage, Model Lsb 0001.
| Device ID | K031321 |
| 510k Number | K031321 |
| Device Name: | LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 |
| Classification | Bandage, Liquid |
| Applicant | MEDLOGIC GLOBAL LIMITED WESTERN WOOD WAY LANGAGE SCIENCE PARK Plymouth, Devon, GB Pl7 5bg |
| Contact | Mel Longhurst |
| Correspondent | Mel Longhurst MEDLOGIC GLOBAL LIMITED WESTERN WOOD WAY LANGAGE SCIENCE PARK Plymouth, Devon, GB Pl7 5bg |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-04-25 |
| Decision Date | 2004-01-21 |
| Summary: | summary |