The following data is part of a premarket notification filed by Columbia Bioscience, Inc. with the FDA for Vca Igm Elisa Test System.
| Device ID | K982352 |
| 510k Number | K982352 |
| Device Name: | VCA IGM ELISA TEST SYSTEM |
| Classification | Epstein-barr Virus, Other |
| Applicant | COLUMBIA BIOSCIENCE, INC. 8775 M CENTRE PARK DR. #559 Columbia, MD 21045 |
| Contact | Norman Jenkins |
| Correspondent | Norman Jenkins COLUMBIA BIOSCIENCE, INC. 8775 M CENTRE PARK DR. #559 Columbia, MD 21045 |
| Product Code | LSE |
| CFR Regulation Number | 866.3235 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-07-06 |
| Decision Date | 1998-11-25 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817273020341 | K982352 | 000 |
| 00817273020327 | K982352 | 000 |
| B3507206100 | K982352 | 000 |