The following data is part of a premarket notification filed by Gc America, Inc. with the FDA for Fit Checker Ii.
Device ID | K032289 |
510k Number | K032289 |
Device Name: | FIT CHECKER II |
Classification | Material, Impression |
Applicant | GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
Contact | Terry L Joritz |
Correspondent | Terry L Joritz GC AMERICA, INC. 3737 WEST 127TH ST. Alsip, IL 60803 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-07-24 |
Decision Date | 2003-10-20 |