The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Syngo, Ct Cardiac Function.
Device ID | K123585 |
510k Number | K123585 |
Device Name: | SYNGO, CT CARDIAC FUNCTION |
Classification | System, X-ray, Tomography, Computed |
Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PKWY. Malvern, PA 19355 -1406 |
Contact | Kimberly Mangum |
Correspondent | Kimberly Mangum SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PKWY. Malvern, PA 19355 -1406 |
Product Code | JAK |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-11-21 |
Decision Date | 2012-12-20 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04056869026336 | K123585 | 000 |
04056869013862 | K123585 | 000 |
04056869007779 | K123585 | 000 |