Diagnostic Hybrids, Inc. · Class II · Cleared Aug 30, 2007
| K-number | K070206 |
| Device name | DIAGNOSTIC HYBRIDS D3 DFA VARICELLA-ZOSTER VIRUS IDENTIFICATION KIT, 01-020000 |
| Applicant | Diagnostic Hybrids, Inc. |
| Product code | GQW |
| Device class | Class II |
| Decision date | Aug 30, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 866.3900 |
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