Fisher & Paykel Electronics , Ltd. · Class II · Cleared Oct 6, 1989
| K-number | K892885 |
| Device name | RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR |
| Applicant | Fisher & Paykel Electronics , Ltd. |
| Product code | BTL |
| Device class | Class II |
| Decision date | Oct 6, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 868.5925 |
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