The following data is part of a premarket notification filed by American Bioproducts Co. with the FDA for At-iii Control Plasma Kit.
Device ID | K955040 |
510k Number | K955040 |
Device Name: | AT-III CONTROL PLASMA KIT |
Classification | Control, Plasma, Abnormal |
Applicant | AMERICAN BIOPRODUCTS CO. 5 CENTURY DR. Parsippany, NJ 07054 |
Contact | Andrew Loc B Le |
Correspondent | Andrew Loc B Le AMERICAN BIOPRODUCTS CO. 5 CENTURY DR. Parsippany, NJ 07054 |
Product Code | GGC |
CFR Regulation Number | 864.5425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-03 |
Decision Date | 1996-01-31 |