The following data is part of a premarket notification filed by Baxter Diagnostics, Inc. with the FDA for Paramax Alcohol Reagent.
Device ID | K934275 |
510k Number | K934275 |
Device Name: | PARAMAX ALCOHOL REAGENT |
Classification | Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method |
Applicant | BAXTER DIAGNOSTICS, INC. P.O. BOX 25101 Santa Ana, CA 92799 |
Contact | Scott Beggins |
Correspondent | Scott Beggins BAXTER DIAGNOSTICS, INC. P.O. BOX 25101 Santa Ana, CA 92799 |
Product Code | DIC |
CFR Regulation Number | 862.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-08-31 |
Decision Date | 1994-04-26 |