The following data is part of a premarket notification filed by Advanced Medical Instruments, Inc. with the FDA for System 7500 Nibp/sa02.
| Device ID | K924910 |
| 510k Number | K924910 |
| Device Name: | SYSTEM 7500 NIBP/SA02 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | ADVANCED MEDICAL INSTRUMENTS, INC. 3061 WEST ALBANY Broken Arrow, OK 74012 |
| Contact | James C Lalicker |
| Correspondent | James C Lalicker ADVANCED MEDICAL INSTRUMENTS, INC. 3061 WEST ALBANY Broken Arrow, OK 74012 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-09-29 |
| Decision Date | 1993-05-13 |