The following data is part of a premarket notification filed by Hycor Biomedical, Inc. with the FDA for Hycor Sentry Drugs Of Abuse Urine Control:.
| Device ID | K890957 |
| 510k Number | K890957 |
| Device Name: | HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: |
| Classification | Drug Mixture Control Materials |
| Applicant | HYCOR BIOMEDICAL, INC. 7272 CHAPMAN AVE. Garden Grove, CA 92841 |
| Contact | Ron Hoover |
| Correspondent | Ron Hoover HYCOR BIOMEDICAL, INC. 7272 CHAPMAN AVE. Garden Grove, CA 92841 |
| Product Code | DIF |
| CFR Regulation Number | 862.3280 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-02-27 |
| Decision Date | 1989-03-09 |