The following data is part of a premarket notification filed by American Bioproducts Co. with the FDA for New Stachrom Protein C Test Kit.
Device ID | K931906 |
510k Number | K931906 |
Device Name: | NEW STACHROM PROTEIN C TEST KIT |
Classification | Test, Qualitative And Quantitative Factor Deficiency |
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 | GGP |
CFR Regulation Number | 864.7290 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-13 |
Decision Date | 1993-11-05 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
03607450006711 | K931906 | 000 |