The following data is part of a premarket notification filed by Allegiance Healthcare Corp. with the FDA for Allegiance Genesis Container System.
Device ID | K983299 |
510k Number | K983299 |
Device Name: | ALLEGIANCE GENESIS CONTAINER SYSTEM |
Classification | Wrap, Sterilization |
Applicant | ALLEGIANCE HEALTHCARE CORP. 1500 WAUKEGAN RD.- K Mcgraw Park, IL 60085 |
Contact | Patricia Sharpe-gregg |
Correspondent | Patricia Sharpe-gregg ALLEGIANCE HEALTHCARE CORP. 1500 WAUKEGAN RD.- K Mcgraw Park, IL 60085 |
Product Code | FRG |
CFR Regulation Number | 880.6850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-21 |
Decision Date | 2000-08-04 |
Summary: | summary |