The following data is part of a premarket notification filed by Metrex Research Corp. with the FDA for Kleenaseptic.
| Device ID | K981023 |
| 510k Number | K981023 |
| Device Name: | KLEENASEPTIC |
| Classification | Disinfectant, Medical Devices |
| Applicant | METREX RESEARCH CORP. 1717 W COLLINS AVE. Orange, CA 92667 |
| Contact | Wendy A Urtel |
| Correspondent | Wendy A Urtel METREX RESEARCH CORP. 1717 W COLLINS AVE. Orange, CA 92667 |
| Product Code | LRJ |
| CFR Regulation Number | 880.6890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-03-19 |
| Decision Date | 1998-04-30 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KLEENASEPTIC 72386621 0935090 Dead/Cancelled |
PREDICTED ENVIRONMENTS, INC. 1971-03-17 |