The following data is part of a premarket notification filed by Agfa Healthcare Corp. with the FDA for Agfa Computed Radiography System With Nx2.x Workstations.
Device ID | K071162 |
510k Number | K071162 |
Device Name: | AGFA COMPUTED RADIOGRAPHY SYSTEM WITH NX2.X WORKSTATIONS |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | AGFA HEALTHCARE CORP. 10 SOUTH ACADEMY ST. Greenville, SC 29601 |
Contact | Jeffery A Jedlicka |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2007-04-26 |
Decision Date | 2007-05-08 |
Summary: | summary |