The following data is part of a premarket notification filed by Diametrics Medical, Inc. with the FDA for Irma Sl Blood Analysis System Lactate Cartridge.
Device ID | K013938 |
510k Number | K013938 |
Device Name: | IRMA SL BLOOD ANALYSIS SYSTEM LACTATE CARTRIDGE |
Classification | Acid, Lactic, Enzymatic Method |
Applicant | DIAMETRICS MEDICAL, INC. 2658 PATTON RD. Saint Paul, MN 55113 |
Contact | Nancy Ring |
Correspondent | Nancy Ring DIAMETRICS MEDICAL, INC. 2658 PATTON RD. Saint Paul, MN 55113 |
Product Code | KHP |
CFR Regulation Number | 862.1450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-28 |
Decision Date | 2002-01-28 |
Summary: | summary |