The following data is part of a premarket notification filed by Hemagen Diagnostics, Inc. with the FDA for Raichem Glucose Uv (liquid).
Device ID | K041052 |
510k Number | K041052 |
Device Name: | RAICHEM GLUCOSE UV (LIQUID) |
Classification | Hexokinase, Glucose |
Applicant | HEMAGEN DIAGNOSTICS, INC. 9033 RED BRANCH RD. Columbia, MD 21045 |
Contact | James J Miller |
Correspondent | James J Miller HEMAGEN DIAGNOSTICS, INC. 9033 RED BRANCH RD. Columbia, MD 21045 |
Product Code | CFR |
CFR Regulation Number | 862.1345 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-19 |
Decision Date | 2004-06-30 |