The following data is part of a premarket notification filed by Gc America, Inc. with the FDA for Iso Functional.
Device ID | K022430 |
510k Number | K022430 |
Device Name: | ISO FUNCTIONAL |
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 | 2002-07-25 |
Decision Date | 2002-10-18 |