The following data is part of a premarket notification filed by American Bioproducts Co. with the FDA for Staclot(r) Pnp Test Kit.
Device ID | K924370 |
510k Number | K924370 |
Device Name: | STACLOT(R) PNP TEST KIT |
Classification | Test, Time, Partial Thromboplastin |
Applicant | AMERICAN BIOPRODUCTS CO. 601 NORTH JEFFERSON RD. Parsippany, NJ 07054 |
Contact | Loc B Le |
Correspondent | Loc B Le AMERICAN BIOPRODUCTS CO. 601 NORTH JEFFERSON RD. Parsippany, NJ 07054 |
Product Code | GGW |
CFR Regulation Number | 864.7925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-28 |
Decision Date | 1993-08-09 |