The following data is part of a premarket notification filed by Endosonics Corp. with the FDA for Microsound 6.6f Diagnostic Imaging Catheter Model 50302, Intravascular Ultrasound Imaging System.
Device ID | K950276 |
510k Number | K950276 |
Device Name: | MICROSOUND 6.6F DIAGNOSTIC IMAGING CATHETER MODEL 50302, INTRAVASCULAR ULTRASOUND IMAGING SYSTEM |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | ENDOSONICS CORP. 3078-B PROSPECT PARK DR. Rancho Cordova, CA 95670 |
Contact | Adam D Savakus |
Correspondent | Adam D Savakus ENDOSONICS CORP. 3078-B PROSPECT PARK DR. Rancho Cordova, CA 95670 |
Product Code | IYO |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-01-23 |
Decision Date | 1995-09-22 |