The following data is part of a premarket notification filed by Analogic Corp. with the FDA for Fetalgard 3000 - Models Ip1, Ip2, Ap2 And Ap3.
| Device ID | K950420 |
| 510k Number | K950420 |
| Device Name: | FETALGARD 3000 - MODELS IP1, IP2, AP2 AND AP3 |
| Classification | System, Monitoring, Perinatal |
| Applicant | ANALOGIC CORP. 8 CENTENNIAL DR. Peabody, MA 01960 |
| Contact | James R Levani |
| Correspondent | James R Levani ANALOGIC CORP. 8 CENTENNIAL DR. Peabody, MA 01960 |
| Product Code | HGM |
| CFR Regulation Number | 884.2740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-01-31 |
| Decision Date | 1995-05-15 |