The following data is part of a premarket notification filed by Euro-diagnostica Ab with the FDA for Immunoscan Anti-myeloperoxidase Antibodies (mpo-anca) Quantitative Kit.
Device ID | K971689 |
510k Number | K971689 |
Device Name: | IMMUNOSCAN ANTI-MYELOPEROXIDASE ANTIBODIES (MPO-ANCA) QUANTITATIVE KIT |
Classification | Test System, Antineutrophil Cytoplasmic Antibodies (anca) |
Applicant | EURO-DIAGNOSTICA AB 155 CIDER MILL RD. Ringoes, NJ 08551 |
Contact | Karl A Posselt |
Correspondent | Karl A Posselt EURO-DIAGNOSTICA AB 155 CIDER MILL RD. Ringoes, NJ 08551 |
Product Code | MOB |
CFR Regulation Number | 866.5660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-05-07 |
Decision Date | 1997-10-29 |