The following data is part of a premarket notification filed by American Bioproducts Co. with the FDA for Staclot La Test Kit.
| Device ID | K923731 |
| 510k Number | K923731 |
| Device Name: | STACLOT LA TEST KIT |
| Classification | Activated 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 | GFO |
| CFR Regulation Number | 864.7925 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-27 |
| Decision Date | 1992-12-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03607450005943 | K923731 | 000 |
| 03607450006001 | K923731 | 000 |