The following data is part of a premarket notification filed by Wiener Laboratories S.a.i.c. with the FDA for Wiener Lab. Creatinina Cinetica Aa.
Device ID | K012065 |
510k Number | K012065 |
Device Name: | WIENER LAB. CREATININA CINETICA AA |
Classification | Enzymatic Method, Creatinine |
Applicant | WIENER LABORATORIES S.A.I.C. 2944 RIOBAMBA Rosario, AR 2000 |
Contact | Viviana Cetola |
Correspondent | Viviana Cetola WIENER LABORATORIES S.A.I.C. 2944 RIOBAMBA Rosario, AR 2000 |
Product Code | JFY |
CFR Regulation Number | 862.1225 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-07-02 |
Decision Date | 2001-10-10 |
Summary: | summary |