510(k) K013938

IRMA SL BLOOD ANALYSIS SYSTEM LACTATE CARTRIDGE by Diametrics Medical, Inc. — Product Code KHP

K013938 is an FDA 510(k) premarket notification submitted by Diametrics Medical, Inc. for the device "IRMA SL BLOOD ANALYSIS SYSTEM LACTATE CARTRIDGE". The FDA issued a decision of Substantially Equivalent on January 28, 2002. The device falls under product code KHP (Acid, Lactic, Enzymatic Method), a Class I device regulated under 21 CFR 862.1450. Diametrics Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 28, 2002
Date Received
November 28, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Lactic, Enzymatic Method
Device Class
Class I
Regulation Number
862.1450
Review Panel
CH
Submission Type