The following data is part of a premarket notification filed by E.i. Dupont De Nemours & Co., Inc. with the FDA for Aca(r) Lactic Dehydrogenase Isoenzyme 1(ld1) Veri.
Device ID | K905820 |
510k Number | K905820 |
Device Name: | ACA(R) LACTIC DEHYDROGENASE ISOENZYME 1(LD1) VERI |
Classification | Calibrator, Primary |
Applicant | E.I. DUPONT DE NEMOURS & CO., INC. DU PONT-BMP22/1152 Wilmington, DE 19880 |
Contact | Christopher Bentsen |
Correspondent | Christopher Bentsen E.I. DUPONT DE NEMOURS & CO., INC. DU PONT-BMP22/1152 Wilmington, DE 19880 |
Product Code | JIS |
CFR Regulation Number | 862.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-12-31 |
Decision Date | 1991-02-26 |