The following data is part of a premarket notification filed by Volcano Corporation with the FDA for Volcano S5/s5i Intravascular Ultrasound Imaging And Pressure System.
Device ID | K123898 |
510k Number | K123898 |
Device Name: | VOLCANO S5/S5I INTRAVASCULAR ULTRASOUND IMAGING AND PRESSURE SYSTEM |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | VOLCANO CORPORATION 2870 KILGORE RD. Rancho Cordova, CA 95670 |
Contact | Jwala Jawharkar |
Correspondent | Jwala Jawharkar VOLCANO CORPORATION 2870 KILGORE RD. Rancho Cordova, CA 95670 |
Product Code | IYO |
Subsequent Product Code | DSA |
Subsequent Product Code | DSK |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-12-18 |
Decision Date | 2013-01-14 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00845225012281 | K123898 | 000 |
00845225012274 | K123898 | 000 |
00845225012106 | K123898 | 000 |