The following data is part of a premarket notification filed by Drtech Corp. with the FDA for Flaatz 750.
Device ID | K080064 |
510k Number | K080064 |
Device Name: | FLAATZ 750 |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | DRTECH CORP. 333-1, SANGDEAWON 1-DONG JUNGWON-GU Seongnam-shi, Gyeonggi-do, KR 462-807 |
Contact | Beom-jin Moon |
Correspondent | Ned Devine UNDERWRITERS LABORATORIES, INC. 333 PFINGSTEN RD. Northbrook, IL 60062 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2008-01-10 |
Decision Date | 2008-01-23 |