Lifecore Biomedical, Inc. · Class II · Cleared May 1, 1991
| K-number | K910432 |
| Device name | HAPSET HYDROXYLAPATITE BONE GRAFT PLASTER |
| Applicant | Lifecore Biomedical, Inc. |
| Product code | LYC |
| Device class | Class II |
| Decision date | May 1, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 872.3930 |
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