The following data is part of a premarket notification filed by Agfa-gevaert Ag with the FDA for Adc Compact Plus.
Device ID | K013138 |
510k Number | K013138 |
Device Name: | ADC COMPACT PLUS |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | AGFA-GEVAERT AG 12300 TWINBROOK PKWY. SUITE 625 Rockville, MD 20852 |
Contact | T. Whit Athey |
Correspondent | T. Whit Athey AGFA-GEVAERT AG 12300 TWINBROOK PKWY. SUITE 625 Rockville, MD 20852 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-09-19 |
Decision Date | 2001-09-28 |
Summary: | summary |