| K-number | K811333 |
| Device name | EC MEDIUM |
| Applicant | Acumedia Manufacturers, Inc. |
| Product code | JSJ |
| Device class | Class I |
| Decision date | May 29, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 866.2360 |
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