Litton Bionetics · Class I · Cleared Mar 16, 1984
| K-number | K834443 |
| Device name | ROTAVIRUS BIO-ENZABEAD SCREEN KIT |
| Applicant | Litton Bionetics |
| Product code | LIQ |
| Device class | Class I |
| Decision date | Mar 16, 1984 |
| Decision | Substantially Equivalent |
| Regulation | 866.3405 |
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