| K-number | K770833 |
| Device name | FLUORETEC-M |
| Applicant | Pfizer, Inc. |
| Product code | GMY |
| Device class | Class I |
| Decision date | Jun 8, 1977 |
| Decision | Substantially Equivalent |
| Regulation | 866.3255 |
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