The following data is part of a premarket notification filed by Biomerieux Sa with the FDA for Vidas Lyme Igm.
Device ID | K122979 |
510k Number | K122979 |
Device Name: | VIDAS LYME IGM |
Classification | Reagent, Borrelia Serological Reagent |
Applicant | BIOMERIEUX SA CHEMIN DE L ORME Marcy L Etoile, FR 69280 |
Contact | Catherine Fritsch |
Correspondent | Catherine Fritsch BIOMERIEUX SA CHEMIN DE L ORME Marcy L Etoile, FR 69280 |
Product Code | LSR |
CFR Regulation Number | 866.3830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-09-26 |
Decision Date | 2013-06-04 |
Summary: | summary |