The following data is part of a premarket notification filed by Med-life, Inc. with the FDA for Anesthecache.
| Device ID | K821307 |
| 510k Number | K821307 |
| Device Name: | ANESTHECACHE |
| Classification | Cabinet, Table And Tray, Anesthesia |
| Applicant | MED-LIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BRY |
| CFR Regulation Number | 868.6100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-05-04 |
| Decision Date | 1982-05-14 |