The following data is part of a premarket notification filed by Pharma-plast Usa, Inc. with the FDA for Pharma-plast Insulin Infusion Set.
Device ID | K884978 |
510k Number | K884978 |
Device Name: | PHARMA-PLAST INSULIN INFUSION SET |
Classification | Pump, Infusion, Insulin |
Applicant | PHARMA-PLAST USA, INC. 1801 MCGILL COLLEGE AVE. SUITE 1470, MONTREAL Canada H3a 2n4, CA |
Contact | Douglas M Bennett |
Correspondent | Douglas M Bennett PHARMA-PLAST USA, INC. 1801 MCGILL COLLEGE AVE. SUITE 1470, MONTREAL Canada H3a 2n4, CA |
Product Code | LZG |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-30 |
Decision Date | 1989-06-21 |