The following data is part of a premarket notification filed by Numed, Inc. with the FDA for Z-med Z-med Ii.
| Device ID | K122012 |
| 510k Number | K122012 |
| Device Name: | Z-MED Z-MED II |
| Classification | Balloon Aortic Valvuloplasty |
| Applicant | NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
| Contact | Nichelle Laflesh |
| Correspondent | Nichelle Laflesh NUMED, INC. 2880 MAIN ST. Hopkinton, NY 12965 |
| Product Code | OZT |
| CFR Regulation Number | 870.1255 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-07-10 |
| Decision Date | 2012-10-04 |
| Summary: | summary |