The following data is part of a premarket notification filed by Mckesson Corp. with the FDA for Consious Sedation (analor P-76).
| Device ID | K760017 |
| 510k Number | K760017 |
| Device Name: | CONSIOUS SEDATION (ANALOR P-76) |
| Classification | Mixer, Breathing Gases, Anesthesia Inhalation |
| Applicant | MCKESSON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BZR |
| CFR Regulation Number | 868.5330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-06-11 |
| Decision Date | 1976-07-20 |