The following data is part of a premarket notification filed by Ray Co., Ltd with the FDA for Rct800.
Device ID | K182805 |
510k Number | K182805 |
Device Name: | RCT800 |
Classification | X-ray, Tomography, Computed, Dental |
Applicant | RAY Co., Ltd 332-7, Samsung 1-ro Hwaseong-si, KR 18380 |
Contact | Changhwan Lee |
Correspondent | Changhwan Lee RAY Co., Ltd 332-7, Samsung 1-ro Hwaseong-si, KR 18380 |
Product Code | OAS |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-10-02 |
Decision Date | 2018-12-14 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08800003004003 | K182805 | 000 |
08800003004164 | K182805 | 000 |
08800003004157 | K182805 | 000 |
08800003004140 | K182805 | 000 |
08800003004133 | K182805 | 000 |
08800003004126 | K182805 | 000 |
08800003004119 | K182805 | 000 |
08800003004102 | K182805 | 000 |
08800003004096 | K182805 | 000 |