The following data is part of a premarket notification filed by Olympus Corp. with the FDA for Olympus Albumin Reagent.
Device ID | K922369 |
510k Number | K922369 |
Device Name: | OLYMPUS ALBUMIN REAGENT |
Classification | Bromcresol Green Dye-binding, Albumin |
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 | CIX |
CFR Regulation Number | 862.1035 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-20 |
Decision Date | 1992-07-17 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
15099590060008 | K922369 | 000 |
15099590020002 | K922369 | 000 |
15099590010010 | K922369 | 000 |