This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Device | QUANTITOPE 125I AFP KIT AND CONTROL SERUM |
Generic Name | Kit, Test, Alpha-fetoprotein For Neural Tube Defects |
Applicant | Bio-Rad Laboratories, Inc. |
Date Received | 1986-03-18 |
Decision Date | 1988-04-21 |
PMA | P800025 |
Supplement | S004 |
Product Code | LOK |
Advisory Committee | Immunology |
Expedited Review | No |
Combination Product | No |
Applicant Address | Bio-Rad Laboratories, Inc. 3 Boulevard Raymond Poincare' marnes-la-coquette 92430 |
Supplement Number | Date | Supplement Type |
---|---|---|
P800025 | Original Filing | |
S005 | 1995-12-21 | Normal 180 Day Track |
S004 | 1986-03-18 | |
S003 | 1985-04-01 | |
S002 | ||
S001 | 1984-01-26 |