| K-number | K012578 |
| Device name | REPROCESSED ENDOSCOPIC TROCAR |
| Applicant | Sterilmed, Inc. |
| Product code | NLM |
| Device class | Class II |
| Decision date | Nov 7, 2001 |
| Decision | Substantially Equivalent |
| Regulation | 876.1500 |
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