The following data is part of a premarket notification filed by Imm Enterprises Ltd. with the FDA for Cat. 9 Anesthesiology Respiratory Dev.
| Device ID | K840313 |
| 510k Number | K840313 |
| Device Name: | CAT. 9 ANESTHESIOLOGY RESPIRATORY DEV |
| Classification | Forceps, Tube Introduction |
| Applicant | IMM ENTERPRISES LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BWB |
| CFR Regulation Number | 868.5780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-01-24 |
| Decision Date | 1984-02-04 |