Baxter Healthcare Corp · Class I · Cleared Aug 4, 1989
| K-number | K894031 |
| Device name | PHARMASEAL GENETIC AMNIOCENTESIS TRAY |
| Applicant | Baxter Healthcare Corp |
| Product code | HIO |
| Device class | Class I |
| Decision date | Aug 4, 1989 |
| Decision | Substantially Equivalent — Same Device |
| Regulation | 884.1550 |
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