The following data is part of a premarket notification filed by Kallestad Diag, A Div. Of Erbamont, Inc. with the FDA for Modified Qm300 Albumin Antibody Pack.
Device ID | K896059 |
510k Number | K896059 |
Device Name: | MODIFIED QM300 ALBUMIN ANTIBODY PACK |
Classification | Albumin, Antigen, Antiserum, Control |
Applicant | KALLESTAD DIAG, A DIV. OF ERBAMONT, INC. 2000 LAKE HAZELTINE DR. Chaska, MN 55318 |
Contact | Jan Nebelsick |
Correspondent | Jan Nebelsick KALLESTAD DIAG, A DIV. OF ERBAMONT, INC. 2000 LAKE HAZELTINE DR. Chaska, MN 55318 |
Product Code | DCF |
CFR Regulation Number | 866.5040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-10-18 |
Decision Date | 1989-11-06 |