The following data is part of a premarket notification filed by Incstar Corp. with the FDA for Incstar Epstein-barr Nuclear Antigen (ebna_ Igg Elisa Kit.
Device ID | K946158 |
510k Number | K946158 |
Device Name: | INCSTAR EPSTEIN-BARR NUCLEAR ANTIGEN (EBNA_ IGG ELISA KIT |
Classification | Test, Antigen, Nuclear, Epstein-barr Virus |
Applicant | INCSTAR CORP. 1990 INDUSTRIAL BLVD. P.O. BOX 285 Stillwater, MN 55082 |
Contact | Mary L Frick |
Correspondent | Mary L Frick INCSTAR CORP. 1990 INDUSTRIAL BLVD. P.O. BOX 285 Stillwater, MN 55082 |
Product Code | LLM |
CFR Regulation Number | 866.3235 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-12-08 |
Decision Date | 1995-06-09 |