| K-number | K892220 |
| Device name | LAMINARIA TENT |
| Applicant | Berkeley Medevices |
| Product code | HDY |
| Device class | Class II |
| Decision date | Jun 14, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 884.4260 |
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