The following data is part of a premarket notification filed by Becton, Dickinson & Co. with the FDA for Bd Viper Instrument.
| Device ID | K023955 |
| 510k Number | K023955 |
| Device Name: | BD VIPER INSTRUMENT |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | BECTON, DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 -0999 |
| Contact | Collen A Kistler |
| Correspondent | Collen A Kistler BECTON, DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 -0999 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-11-27 |
| Decision Date | 2003-06-24 |
| Summary: | summary |