Mizuho America, Inc. · Class II · Cleared Sep 12, 1996
| K-number | K955012 |
| Device name | MIZUHO RADIOLUCENT HEAD FRAME |
| Applicant | Mizuho America, Inc. |
| Product code | HBL |
| Device class | Class II |
| Decision date | Sep 12, 1996 |
| Decision | Substantially Equivalent |
| Regulation | 882.4460 |
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