The following data is part of a premarket notification filed by Todd Industries, Inc. with the FDA for Venturi Mask/delivery System #6078.
| Device ID | K810430 |
| 510k Number | K810430 |
| Device Name: | VENTURI MASK/DELIVERY SYSTEM #6078 |
| Classification | Mask, Oxygen, Low Concentration, Venturi |
| Applicant | TODD INDUSTRIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BYF |
| CFR Regulation Number | 868.5600 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-19 |
| Decision Date | 1981-03-13 |