The following data is part of a premarket notification filed by Clark Laboratories, Inc. with the FDA for Ea-d Igg Elisa Test System.
| Device ID | K973123 |
| 510k Number | K973123 |
| Device Name: | EA-D IGG ELISA TEST SYSTEM |
| Classification | Epstein-barr Virus, Other |
| Applicant | CLARK LABORATORIES, INC. 1306F BAILES LN. Frederick, MD 21701 |
| Contact | William L Boteler |
| Correspondent | William L Boteler CLARK LABORATORIES, INC. 1306F BAILES LN. Frederick, MD 21701 |
| Product Code | LSE |
| CFR Regulation Number | 866.3235 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-20 |
| Decision Date | 1998-03-26 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05391516743365 | K973123 | 000 |
| 05391516746564 | K973123 | 000 |