The following data is part of a premarket notification filed by American Bioproducts Co. with the FDA for Asserachrom Vwf Kit.
| Device ID | K860371 |
| 510k Number | K860371 |
| Device Name: | ASSERACHROM VWF KIT |
| Classification | Test, Qualitative And Quantitative Factor Deficiency |
| Applicant | AMERICAN BIOPRODUCTS CO. 601 NORTH JEFFERSON RD. Parsippany, NJ 07054 |
| Contact | Loc B Le,phd |
| Correspondent | Loc B Le,phd AMERICAN BIOPRODUCTS CO. 601 NORTH JEFFERSON RD. Parsippany, NJ 07054 |
| Product Code | GGP |
| CFR Regulation Number | 864.7290 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-02-03 |
| Decision Date | 1986-04-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03607450009422 | K860371 | 000 |