L H M Ent., Inc. · Class II · Cleared Feb 15, 1990
| K-number | K900439 |
| Device name | SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CC |
| Applicant | L H M Ent., Inc. |
| Product code | FIH |
| Device class | Class II |
| Decision date | Feb 15, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 876.5820 |
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