The following data is part of a premarket notification filed by Olympus America, Inc. with the FDA for Olympus Serum Protein Multicalibrator 2.
Device ID | K992086 |
510k Number | K992086 |
Device Name: | OLYMPUS SERUM PROTEIN MULTICALIBRATOR 2 |
Classification | Calibrator, Multi-analyte Mixture |
Applicant | OLYMPUS AMERICA, INC. TWO CORPORATE CENTER DR. Melville, NY 11747 -3157 |
Contact | Laura Storms-tyler |
Correspondent | Laura Storms-tyler OLYMPUS AMERICA, INC. TWO CORPORATE CENTER DR. Melville, NY 11747 -3157 |
Product Code | JIX |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-06-21 |
Decision Date | 1999-08-19 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
15099590080785 | K992086 | 000 |