The following data is part of a premarket notification filed by Cooper-hewitt Electric Co. with the FDA for Aquanomics, #mp2sf.
| Device ID | K813048 |
| 510k Number | K813048 |
| Device Name: | AQUANOMICS, #MP2SF |
| Classification | Purifier, Water, Ultraviolet, Medical |
| Applicant | COOPER-HEWITT ELECTRIC CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KMG |
| CFR Regulation Number | 880.6710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-10-28 |
| Decision Date | 1981-12-02 |