The following data is part of a premarket notification filed by Hill-rom Manufacturing, Inc. with the FDA for Modification To Watchchild Obstetrical Patient Data Management System (also Referred To As) The Watchchild System.
| Device ID | K032772 |
| 510k Number | K032772 |
| Device Name: | MODIFICATION TO WATCHCHILD OBSTETRICAL PATIENT DATA MANAGEMENT SYSTEM (ALSO REFERRED TO AS) THE WATCHCHILD SYSTEM |
| Classification | System, Monitoring, Perinatal |
| Applicant | HILL-ROM MANUFACTURING, INC. 1225 CRESCENT GREEN SUITE 200 Cary, NC 27511 |
| Contact | Cindy L Crosby |
| Correspondent | Cindy L Crosby HILL-ROM MANUFACTURING, INC. 1225 CRESCENT GREEN SUITE 200 Cary, NC 27511 |
| Product Code | HGM |
| CFR Regulation Number | 884.2740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-08 |
| Decision Date | 2003-10-08 |
| Summary: | summary |