The following data is part of a premarket notification filed by Olympus America, Inc. with the FDA for Olympus Ldl Cholesterol Reagent, Osr6196/osr6296; Olympus Ldl Cholesterol Calibrator, Odc0024.
Device ID | K040471 |
510k Number | K040471 |
Device Name: | OLYMPUS LDL CHOLESTEROL REAGENT, OSR6196/OSR6296; OLYMPUS LDL CHOLESTEROL CALIBRATOR, ODC0024 |
Classification | Calibrator, Secondary |
Applicant | OLYMPUS AMERICA, INC. 3131 WEST ROYAL LN. Irving, TX 75063 -3104 |
Contact | Michael Campbell |
Correspondent | Michael Campbell OLYMPUS AMERICA, INC. 3131 WEST ROYAL LN. Irving, TX 75063 -3104 |
Product Code | JIT |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-02-24 |
Decision Date | 2004-03-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
15099590070519 | K040471 | 000 |
15099590020361 | K040471 | 000 |
15099590010928 | K040471 | 000 |