The following data is part of a premarket notification filed by Cooperbiomedical, Inc. with the FDA for Immuno-plate Iv Radial Immuno Test Kit/human Hapto.
Device ID | K864512 |
510k Number | K864512 |
Device Name: | IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO |
Classification | Haptoglobin, Antigen, Antiserum, Control |
Applicant | COOPERBIOMEDICAL, INC. ONE TECHNOLOGY COURT Malvern, PA 19355 |
Contact | Brewster, Phd |
Correspondent | Brewster, Phd COOPERBIOMEDICAL, INC. ONE TECHNOLOGY COURT Malvern, PA 19355 |
Product Code | DAD |
CFR Regulation Number | 866.5460 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-11-13 |
Decision Date | 1987-02-13 |