The following data is part of a premarket notification filed by Sweden Diagnostics (germany) Gmbh with the FDA for Varelisa Gliadin Igg Antibodies.
Device ID | K041357 |
510k Number | K041357 |
Device Name: | VARELISA GLIADIN IGG ANTIBODIES |
Classification | Antibodies, Gliadin |
Applicant | SWEDEN DIAGNOSTICS (GERMANY) GMBH MUNZINGER STRASSE 7 Freiburg, DE D-79111 |
Contact | Michael Linss |
Correspondent | Michael Linss SWEDEN DIAGNOSTICS (GERMANY) GMBH MUNZINGER STRASSE 7 Freiburg, DE D-79111 |
Product Code | MST |
CFR Regulation Number | 866.5750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-20 |
Decision Date | 2004-08-02 |
Summary: | summary |