The following data is part of a premarket notification filed by Diamedix Corp. with the FDA for Anti-dnp Microassay.
Device ID | K872560 |
510k Number | K872560 |
Device Name: | ANTI-DNP MICROASSAY |
Classification | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control |
Applicant | DIAMEDIX CORP. 2140 NORTH MIAMI AVE. Miami, FL 33127 |
Contact | Kiefer, Phd |
Correspondent | Kiefer, Phd DIAMEDIX CORP. 2140 NORTH MIAMI AVE. Miami, FL 33127 |
Product Code | DHN |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-29 |
Decision Date | 1987-07-21 |