The following data is part of a premarket notification filed by Calgon Vestal Div. with the FDA for Bill Evans-klenz.
Device ID | K944033 |
510k Number | K944033 |
Device Name: | BILL EVANS-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 | 1994-08-17 |
Decision Date | 1994-10-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BILL EVANS-KLENZ 74135508 1731983 Dead/Cancelled |
STERIS CORPORATION 1991-01-30 |