PAJUNK GmbH Medizintechnologie · Class II · Cleared Feb 14, 2007
| K-number | K063697 |
| Device name | SPECIAL SPROTTE, CHIBA, DR STEINHOFF KIT |
| Applicant | PAJUNK GmbH Medizintechnologie |
| Product code | KNW |
| Device class | Class II |
| Decision date | Feb 14, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 876.1075 |
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