The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Hitachi 704.
| Device ID | K854025 |
| 510k Number | K854025 |
| Device Name: | HITACHI 704 |
| Classification | Analyzer, Chemistry (photometric, Discrete), For Clinical Use |
| Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Contact | Sue Smith |
| Correspondent | Sue Smith BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Product Code | JJE |
| CFR Regulation Number | 862.2160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-09-30 |
| Decision Date | 1985-10-28 |