The following data is part of a premarket notification filed by Hitachi Medical Corp. Of America with the FDA for Electronic Ultrasound Scanner Eub-315, Modified.
Device ID | K912364 |
510k Number | K912364 |
Device Name: | ELECTRONIC ULTRASOUND SCANNER EUB-315, MODIFIED |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | HITACHI MEDICAL CORP. OF AMERICA 50 PROSPECT AVE. Tarrytown, NY 10591 |
Contact | Takiguchi |
Correspondent | Takiguchi HITACHI MEDICAL CORP. OF AMERICA 50 PROSPECT AVE. Tarrytown, NY 10591 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-05-29 |
Decision Date | 1992-08-26 |