The following data is part of a premarket notification filed by Millipore Corp. with the FDA for Millex Vv, Gv, And Hv Syringe Filter Units.
| Device ID | K023892 |
| 510k Number | K023892 |
| Device Name: | MILLEX VV, GV, AND HV SYRINGE FILTER UNITS |
| Classification | Filter, Conduction, Anesthetic |
| Applicant | MILLIPORE CORP. 80 ASHBY RD. Bedford, MA 01730 |
| Contact | Thomas Borrows |
| Correspondent | Thomas Borrows MILLIPORE CORP. 80 ASHBY RD. Bedford, MA 01730 |
| Product Code | BSN |
| CFR Regulation Number | 868.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-11-22 |
| Decision Date | 2003-01-17 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04054839076770 | K023892 | 000 |
| 04054839076725 | K023892 | 000 |
| 04054839076558 | K023892 | 000 |