The following data is part of a premarket notification filed by Sporicidin Intl. with the FDA for Sporicidin Brand Disinfectant Solution.
| Device ID | K904581 |
| 510k Number | K904581 |
| Device Name: | SPORICIDIN BRAND DISINFECTANT SOLUTION |
| Classification | Disinfectant, Medical Devices |
| Applicant | SPORICIDIN INTL. 5901 MONTROSE RD. Rockville, MD 20852 |
| Contact | Edward G Faeth |
| Correspondent | Edward G Faeth SPORICIDIN INTL. 5901 MONTROSE RD. Rockville, MD 20852 |
| Product Code | LRJ |
| CFR Regulation Number | 880.6890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-09 |
| Decision Date | 1992-05-18 |