The following data is part of a premarket notification filed by Convertors with the FDA for Mask, Surgical.
| Device ID | K780169 |
| 510k Number | K780169 |
| Device Name: | MASK, SURGICAL |
| Classification | Mask, Surgical |
| Applicant | CONVERTORS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FXX |
| CFR Regulation Number | 878.4040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-02 |
| Decision Date | 1978-02-13 |