The following data is part of a premarket notification filed by Adrem Technology Sarl with the FDA for Veinoplus Neuromuscular Stimulator.
| Device ID | K072252 |
| 510k Number | K072252 |
| Device Name: | VEINOPLUS NEUROMUSCULAR STIMULATOR |
| Classification | Stimulator, Muscle, Powered |
| Applicant | ADREM TECHNOLOGY SARL 9109 COPENHAVER DRIVE Potomac, MD 20854 |
| Contact | Norman F Estrin |
| Correspondent | Norman F Estrin ADREM TECHNOLOGY SARL 9109 COPENHAVER DRIVE Potomac, MD 20854 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-08-13 |
| Decision Date | 2008-01-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03701084900022 | K072252 | 000 |
| 03701084900015 | K072252 | 000 |