The following data is part of a premarket notification filed by Olympus Corp. with the FDA for Olympus Calcium Reagent.
Device ID | K924435 |
510k Number | K924435 |
Device Name: | OLYMPUS CALCIUM REAGENT |
Classification | Cresolphthalein Complexone, Calcium |
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 | CIC |
CFR Regulation Number | 862.1145 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-01 |
Decision Date | 1992-10-19 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
15099590020057 | K924435 | 000 |
15099590010126 | K924435 | 000 |