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 |