The following data is part of a premarket notification filed by Meridian Medical Systems, Llc with the FDA for Universal Digital Interface Wireless - Udi 1417w.
Device ID | K111305 |
510k Number | K111305 |
Device Name: | UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | MERIDIAN MEDICAL SYSTEMS, LLC 325 HARRIS DRIVE Aurora, OH 44202 |
Contact | Ariel Marciano |
Correspondent | Ariel Marciano MERIDIAN MEDICAL SYSTEMS, LLC 325 HARRIS DRIVE Aurora, OH 44202 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-05-09 |
Decision Date | 2012-01-31 |