The following data is part of a premarket notification filed by Bailey Medical Engineering with the FDA for Nurture Iii.
| Device ID | K924312 |
| 510k Number | K924312 |
| Device Name: | NURTURE III |
| Classification | Pump, Breast, Powered |
| Applicant | BAILEY MEDICAL ENGINEERING 1820 DONNA AVE. Los Osos, CA 93402 |
| Contact | Barry Bailey |
| Correspondent | Barry Bailey BAILEY MEDICAL ENGINEERING 1820 DONNA AVE. Los Osos, CA 93402 |
| Product Code | HGX |
| CFR Regulation Number | 884.5160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-26 |
| Decision Date | 1995-05-11 |