Stortford Medical, LLC · Class II · Cleared May 1, 2009
| K-number | K090308 |
| Device name | RESTEP DVY SYSTEM, MODEL RSP-101 |
| Applicant | Stortford Medical, LLC |
| Product code | JOW |
| Device class | Class II |
| Decision date | May 1, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 870.5800 |
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