The following data is part of a premarket notification filed by Beckman Instruments, Inc. with the FDA for Meter, Iv Ph, Model Expandomatic.
| Device ID | K770352 |
| 510k Number | K770352 |
| Device Name: | METER, IV PH, MODEL EXPANDOMATIC |
| Classification | Ph Meter |
| Applicant | BECKMAN INSTRUMENTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JQY |
| CFR Regulation Number | 862.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-02-22 |
| Decision Date | 1977-04-08 |