The following data is part of a premarket notification filed by Olympus Corp. with the FDA for Olympus Ggt Reagent.
Device ID | K922230 |
510k Number | K922230 |
Device Name: | OLYMPUS GGT REAGENT |
Classification | Kinetic Method, Gamma-glutamyl Transpeptidase |
Applicant | OLYMPUS CORP. 4 NEVADA DR. Lake Success, NY 11042 |
Contact | Laura Storms-tyler |
Correspondent | Laura Storms-tyler OLYMPUS CORP. 4 NEVADA DR. Lake Success, NY 11042 |
Product Code | JQB |
CFR Regulation Number | 862.1360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-12 |
Decision Date | 1992-06-25 |