The following data is part of a premarket notification filed by Advanced Technology Laboratories, Inc. with the FDA for Fetalert Adr Fetal Monitor.
| Device ID | K871383 |
| 510k Number | K871383 |
| Device Name: | FETALERT ADR FETAL MONITOR |
| Classification | System, Monitoring, Perinatal |
| Applicant | ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
| Contact | John Dellinger |
| Correspondent | John Dellinger ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
| Product Code | HGM |
| CFR Regulation Number | 884.2740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-07 |
| Decision Date | 1987-06-01 |