The following data is part of a premarket notification filed by Hitachi Medical Corp. Of America with the FDA for Eup-f124 5.0 Mhz Convex Array Finger Top Probe.
| Device ID | K890531 |
| 510k Number | K890531 |
| Device Name: | EUP-F124 5.0 MHZ CONVEX ARRAY FINGER TOP 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 |