The following data is part of a premarket notification filed by Concord Laboratories, Inc. with the FDA for Alcohol Swabs.
| Device ID | K833993 |
| 510k Number | K833993 |
| Device Name: | ALCOHOL SWABS |
| Classification | Pad, Alcohol, Device Disinfectant |
| Applicant | CONCORD LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LKB |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-21 |
| Decision Date | 1984-01-30 |