| K-number | K091412 |
| Device name | CLEAN PEAK FLOW METER |
| Applicant | Viasys Healthcare GmbH |
| Product code | BZH |
| Device class | Class II |
| Decision date | Aug 21, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 868.1860 |
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