The following data is part of a premarket notification filed by Advanced Instrumentations, Inc. with the FDA for Fm-1000 Plus Fetal Monitor.
| Device ID | K112187 |
| 510k Number | K112187 |
| Device Name: | FM-1000 PLUS FETAL MONITOR |
| Classification | System, Monitoring, Perinatal |
| Applicant | ADVANCED INSTRUMENTATIONS, INC. 601 W 20 ST Hialeah, FL 33010 |
| Contact | Jorge Millan |
| Correspondent | Jorge Millan ADVANCED INSTRUMENTATIONS, INC. 601 W 20 ST Hialeah, FL 33010 |
| Product Code | HGM |
| CFR Regulation Number | 884.2740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-07-29 |
| Decision Date | 2011-09-21 |
| Summary: | summary |