The following data is part of a premarket notification filed by Careray Digital Medical System Co., Ltd. with the FDA for Careview 1800l.
Device ID | K153492 |
510k Number | K153492 |
Device Name: | CareView 1800L |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | CARERAY DIGITAL MEDICAL SYSTEM CO., LTD. A2-201/B3-501, BIOBAY, 218 XINGHU STREET, SUZHOU INDUSTRIAL PARK Suzhou, CN 215123 |
Contact | Leilei Li |
Correspondent | Leilei Li CARERAY DIGITAL MEDICAL SYSTEM CO., LTD. A2-201/B3-501, BIOBAY, 218 XINGHU STREET, SUZHOU INDUSTRIAL PARK Suzhou, CN 215123 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-12-04 |
Decision Date | 2015-12-24 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06970597830240 | K153492 | 000 |