Hirata Sangyo Co. USA, Inc. · Class II · Cleared Oct 18, 1982
| K-number | K821989 |
| Device name | NON-STETHO 7, UM-15TP |
| Applicant | Hirata Sangyo Co. USA, Inc. |
| Product code | DXN |
| Device class | Class II |
| Decision date | Oct 18, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 870.1130 |
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