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 |