The following data is part of a premarket notification filed by Acon Laboratories, Inc. with the FDA for Acon Amp 300 One Step Amphetamine Test Strip And Device.
Device ID | K041822 |
510k Number | K041822 |
Device Name: | ACON AMP 300 ONE STEP AMPHETAMINE TEST STRIP AND DEVICE |
Classification | Enzyme Immunoassay, Amphetamine |
Applicant | ACON LABORATORIES, INC. 4108 SORRENTO VALLEY BLVD. San Diego, CA 92121 |
Contact | Edward Tung |
Correspondent | Edward Tung ACON LABORATORIES, INC. 4108 SORRENTO VALLEY BLVD. San Diego, CA 92121 |
Product Code | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-07-06 |
Decision Date | 2004-09-16 |
Summary: | summary |