The following data is part of a premarket notification filed by Anticancer Inc with the FDA for A/c Enzymatic Homocysteine Assay.
Device ID | K030754 |
510k Number | K030754 |
Device Name: | A/C ENZYMATIC HOMOCYSTEINE ASSAY |
Classification | Urinary Homocystine (nonquantitative) Test System |
Applicant | ANTICANCER INC 7917 OSTROW ST. San Diego, CA 92111 |
Contact | Yuying Tan |
Correspondent | Yuying Tan ANTICANCER INC 7917 OSTROW ST. San Diego, CA 92111 |
Product Code | LPS |
CFR Regulation Number | 862.1377 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-03-10 |
Decision Date | 2003-07-11 |
Summary: | summary |