The following data is part of a premarket notification filed by Via Medical Corp. with the FDA for Via 1-01 Infusion Pump/blood Chem. Syst. -- Mod..
| Device ID | K922997 |
| 510k Number | K922997 |
| Device Name: | VIA 1-01 INFUSION PUMP/BLOOD CHEM. SYST. -- MOD. |
| Classification | Pump, Infusion, Analytical Sampling |
| Applicant | VIA MEDICAL CORP. 10633 ROSELLE ST. San Diego, CA 92121 |
| Contact | Dan Mckay |
| Correspondent | Dan Mckay VIA MEDICAL CORP. 10633 ROSELLE ST. San Diego, CA 92121 |
| Product Code | LZF |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-22 |
| Decision Date | 1994-01-11 |