The following data is part of a premarket notification filed by E.i. Dupont De Nemours & Co., Inc. with the FDA for Dimension(r) Xl Clinical Chemistry System.
Device ID | K944093 |
510k Number | K944093 |
Device Name: | DIMENSION(R) XL CLINICAL CHEMISTRY SYSTEM |
Classification | Analyzer, Chemistry (photometric, Discrete), For Clinical Use |
Applicant | E.I. DUPONT DE NEMOURS & CO., INC. MEDICAL PRODUCTS DEPARTMENT BARLEY MILL PLAZA, P22-1170 Wilmington, DE 19898 |
Contact | Carolyn K George |
Correspondent | Carolyn K George E.I. DUPONT DE NEMOURS & CO., INC. MEDICAL PRODUCTS DEPARTMENT BARLEY MILL PLAZA, P22-1170 Wilmington, DE 19898 |
Product Code | JJE |
CFR Regulation Number | 862.2160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-08-22 |
Decision Date | 1994-11-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00842768004865 | K944093 | 000 |