Smith & Nephew Dyonics, Inc. · Class II · Cleared Aug 19, 1994
| K-number | K936071 |
| Device name | SMITH & NEPHEW DYONICS INC. ELECTRONIC ENDOSCOPE |
| Applicant | Smith & Nephew Dyonics, Inc. |
| Product code | HET |
| Device class | Class II |
| Decision date | Aug 19, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 884.1720 |
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