The following data is part of a premarket notification filed by Kallestad Diag, A Div. Of Erbamont, Inc. with the FDA for Lp 400 Microplate Reader.
Device ID | K894859 |
510k Number | K894859 |
Device Name: | LP 400 MICROPLATE READER |
Classification | Colorimeter, Photometer, Spectrophotometer For Clinical Use |
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 | JJQ |
CFR Regulation Number | 862.2300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-07-31 |
Decision Date | 1989-10-31 |