The following data is part of a premarket notification filed by Sage Products, Inc. with the FDA for Sage 2200 Sterile Specimen Container.
| Device ID | K813408 |
| 510k Number | K813408 |
| Device Name: | SAGE 2200 STERILE SPECIMEN CONTAINER |
| Classification | Warmer, Infant Radiant |
| Applicant | SAGE PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FMT |
| CFR Regulation Number | 880.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-07 |
| Decision Date | 1982-01-25 |