The following data is part of a premarket notification filed by Hitachi Medical Corp. Of America with the FDA for Eup-c321 5.0mhz Convex Type Probe.
Device ID | K890532 |
510k Number | K890532 |
Device Name: | EUP-C321 5.0MHZ CONVEX TYPE PROBE |
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 | 1989-02-02 |
Decision Date | 1990-04-13 |