The following data is part of a premarket notification filed by Agfa Healthcare N.v. with the FDA for Icis View.
Device ID | K143397 |
510k Number | K143397 |
Device Name: | ICIS View |
Classification | System, Image Processing, Radiological |
Applicant | Agfa HealthCare N.V. Septestraat 27 Mortsel, BE B-2640 |
Contact | Jodi Coleman |
Correspondent | Shaeann Cavanagh AGFA Healthcare 10 South Academy Street Greenville, SC 29601 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-26 |
Decision Date | 2015-06-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05414904252444 | K143397 | 000 |
05414904242919 | K143397 | 000 |
05414904218532 | K143397 | 000 |