The following data is part of a premarket notification filed by Fujifilm Sonosite,inc. with the FDA for Sonosite Maxx Series Ultrasound System.
Device ID | K130173 |
510k Number | K130173 |
Device Name: | SONOSITE MAXX SERIES ULTRASOUND SYSTEM |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | FUJIFILM SONOSITE,INC. 21919 30th Dr SE Bothell, WA 98021 |
Contact | Scott Paulson |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | IYN |
Subsequent Product Code | ITX |
Subsequent Product Code | IYO |
Subsequent Product Code | LLZ |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2013-01-24 |
Decision Date | 2013-03-25 |
Summary: | summary |