The following data is part of a premarket notification filed by Ameritek, Inc. with the FDA for Dbest Amphetamines Test Kit.
Device ID | K981504 |
510k Number | K981504 |
Device Name: | DBEST AMPHETAMINES TEST KIT |
Classification | Enzyme Immunoassay, Amphetamine |
Applicant | AMERITEK, INC. 7030 35TH AVE., N.E. Seattle, WA 98115 |
Contact | K.c. Yee |
Correspondent | K.c. Yee AMERITEK, INC. 7030 35TH AVE., N.E. Seattle, WA 98115 |
Product Code | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-04-27 |
Decision Date | 1998-08-06 |