The following data is part of a premarket notification filed by Agfa Healthcare Corp. with the FDA for Orthopedic Software For Impax Workstations.
Device ID | K071972 |
510k Number | K071972 |
Device Name: | ORTHOPEDIC SOFTWARE FOR IMPAX WORKSTATIONS |
Classification | System, Image Processing, Radiological |
Applicant | AGFA HEALTHCARE CORP. 10 SOUTH ACADEMY ST. Greenville, SC 29601 |
Contact | Tom Holbrook |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2007-07-17 |
Decision Date | 2007-07-30 |
Summary: | summary |