The following data is part of a premarket notification filed by Chesebrough-pond's U.s.a. Co. with the FDA for Nebulization Kit & Adapter Kit.
| Device ID | K780264 |
| 510k Number | K780264 |
| Device Name: | NEBULIZATION KIT & ADAPTER KIT |
| Classification | Nebulizer (direct Patient Interface) |
| Applicant | CHESEBROUGH-POND'S U.S.A. CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAF |
| CFR Regulation Number | 868.5630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-17 |
| Decision Date | 1978-03-09 |