The following data is part of a premarket notification filed by Biosound, Inc. with the FDA for Biopsy Accessories For Ultrasound Probes.
Device ID | K912088 |
510k Number | K912088 |
Device Name: | BIOPSY ACCESSORIES FOR ULTRASOUND PROBES |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | BIOSOUND, INC. 7990 CASTLEWAY DR. P.O. BOX 50867 Indianapolis, IN 46250 |
Contact | Carri Stichnoth |
Correspondent | Carri Stichnoth BIOSOUND, INC. 7990 CASTLEWAY DR. P.O. BOX 50867 Indianapolis, IN 46250 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-13 |
Decision Date | 1991-12-05 |