| K-number | K821671 |
| Device name | DISPO. AES. |
| Applicant | Hiraoka New York, Inc. |
| Product code | FMF |
| Device class | Class II |
| Decision date | Jul 28, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 880.5860 |
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