Johnson & Johnson Professionals, Inc. · Class II · Cleared Apr 4, 1979
| K-number | K790341 |
| Device name | DELTA-NET |
| Applicant | Johnson & Johnson Professionals, Inc. |
| Product code | KKX |
| Device class | Class II |
| Decision date | Apr 4, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 878.4370 |
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