The following data is part of a premarket notification filed by Calgon Vestal Div. with the FDA for Alsa-klenz.
Device ID | K944494 |
510k Number | K944494 |
Device Name: | ALSA-KLENZ |
Classification | Cleaner, Ultrasonic, Medical Instrument |
Applicant | CALGON VESTAL DIV. P.O. BOX 147 St.louis, MO 63166 -0147 |
Contact | Susie Amberger |
Correspondent | Susie Amberger CALGON VESTAL DIV. P.O. BOX 147 St.louis, MO 63166 -0147 |
Product Code | FLG |
CFR Regulation Number | 880.6150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-09-13 |
Decision Date | 1994-10-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALSA-KLENZ 74139958 1714582 Dead/Cancelled |
STERIS CORPORATION 1991-02-19 |