Philips Ultrasound, Inc. · Class II · Cleared May 15, 2012
| K-number | K121223 |
| Device name | QLAB WITH FHN AND VPQ PLUG-IN |
| Applicant | Philips Ultrasound, Inc. |
| Product code | LLZ |
| Device class | Class II |
| Decision date | May 15, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 892.2050 |
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