The following data is part of a premarket notification filed by Travenol Laboratories, S.a. with the FDA for Volumetric Pump Admin. Sets.
Device ID | K830017 |
510k Number | K830017 |
Device Name: | VOLUMETRIC PUMP ADMIN. SETS |
Classification | Pump, Infusion |
Applicant | TRAVENOL LABORATORIES, S.A. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-01-03 |
Decision Date | 1983-01-26 |