Princeton BioMeditech Corp. · Class I · Cleared Nov 25, 1998
| K-number | K983386 |
| Device name | BIOSTREP A-DIRECT STREP A ANTIGEN TEST |
| Applicant | Princeton BioMeditech Corp. |
| Product code | GTY |
| Device class | Class I |
| Decision date | Nov 25, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 866.3740 |
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