The following data is part of a premarket notification filed by New Medical Co., Ltd. with the FDA for Saturn 9000-550.
Device ID | K072984 |
510k Number | K072984 |
Device Name: | SATURN 9000-550 |
Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
Applicant | NEW MEDICAL CO., LTD. 4F, NO.42, SINGZHONG RD. NEIHU DISTRICT Taipei, TW 114 |
Contact | Young-hoon Shin |
Correspondent | Young-hoon Shin NEW MEDICAL CO., LTD. 4F, NO.42, SINGZHONG RD. NEIHU DISTRICT Taipei, TW 114 |
Product Code | MQB |
CFR Regulation Number | 892.1680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-23 |
Decision Date | 2007-11-14 |
Summary: | summary |