Sonicaid, Inc. · Class I · Cleared Oct 27, 1983
| K-number | K833227 |
| Device name | SONICAID MODEL D206E AIR EMBOLI-DETECT |
| Applicant | Sonicaid, Inc. |
| Product code | LBA |
| Device class | Class I |
| Decision date | Oct 27, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 862.3280 |
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