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 |