The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Ssa-770a, Aplio Version 5.5.
Device ID | K041499 |
510k Number | K041499 |
Device Name: | SSA-770A, APLIO VERSION 5.5 |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | TOSHIBA MEDICAL SYSTEMS CORPORATION 2441 MICHELLE DRIVE Tustin, CA 92780 |
Contact | Paul Biggins |
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 |
CFR Regulation Number | 892.1550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2004-06-07 |
Decision Date | 2004-06-10 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04987670001802 | K041499 | 000 |
04987670001284 | K041499 | 000 |
04987670001277 | K041499 | 000 |
04987670001246 | K041499 | 000 |
04987670000942 | K041499 | 000 |
04987670000911 | K041499 | 000 |