Medlogic Global Limited · Class I · Cleared Jan 13, 2003
| K-number | K023163 |
| Device name | LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020 |
| Applicant | Medlogic Global Limited |
| Product code | KMF |
| Device class | Class I |
| Decision date | Jan 13, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 880.5090 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov