Tucker & Associates · Class I · Cleared May 4, 1998
| K-number | K980827 |
| Device name | LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING |
| Applicant | Tucker & Associates |
| Product code | LZB |
| Device class | Class I |
| Decision date | May 4, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 880.6250 |
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